المؤلفون: Abraham Daniel, Ann, Silzer, Talisa, Sun, Jie, Zhou, Zhengyang, Hall, Courtney, Phillips, Nicole, Barber, Robert C.

المصدر: Journal of Alzheimer's Disease

مصطلحات موضوعية: Alzheimer's disease, Mexican Americans, epigenetics, methylation, mild cognitive impairment, Aged, Humans, Cognitive Dysfunction / blood, Cognitive Dysfunction / epidemiology, Cognitive Dysfunction / ethnology, Cognitive Dysfunction / genetics, CREB-Binding Protein / blood, CREB-Binding Protein / genetics, DNA Methylation / genetics, Epigenesis, Genetic / genetics, Genetic Predisposition to Disease / epidemiology, Genetic Predisposition to Disease / ethnology, Genetic Predisposition to Disease / genetics, Mexican Americans / genetics, Minority Groups, Risk Factors, White / genetics

وصف الملف: application/pdf

العلاقة: https://doi.org/10.3233/JAD-221031Test; Abraham Daniel, A., Silzer, T., Sun, J., Zhou, Z., Hall, C., Phillips, N., & Barber, R. (2023). Hypermethylation at CREBBP Is Associated with Cognitive Impairment in a Mexican American Cohort. Journal of Alzheimer's disease : JAD, 92(4), 1229-1239. https://doi.org/10.3233/JAD-221031Test; https://hdl.handle.net/20.500.12503/32365Test; 92

الإتاحة: https://doi.org/20.500.12503/32365Test
https://doi.org/10.3233/JAD-221031Test
https://hdl.handle.net/20.500.12503/32365Test

المساهمون: Kwang Yoon Kim, Jung Oh Kim, Young-Sang Kim, Ja-Eun Choi, Jae-Min Park, Kunhee Han, Da-Hyun Park, Yon Chul Park, Bom Taeck Kim, Kyung-Won Hong, Park, Jae Min

مصطلحات موضوعية: Adult, Aged, Alcohol Drinking / epidemiology, Alleles, Case-Control Studies, DNA-Binding Proteins / genetics, Female, Genetic Predisposition to Disease / epidemiology, Genome-Wide Association Study, Hepatocyte Nuclear Factor 1-alpha / genetics, Humans, Liver Diseases, Alcoholic / epidemiology, Alcoholic / genetics, Male, Middle Aged, Polymorphism, Single Nucleotide, Republic of Korea / epidemiology, Risk Assessment, Risk Factors, gamma-Glutamyltransferase / genetics

العلاقة: HEPATOLOGY; J00985; OAK-2022-00554; https://ir.ymlib.yonsei.ac.kr/handle/22282913/187980Test; T202200382; HEPATOLOGY, Vol.75(2) : 391-402, 2022-02

الإتاحة: https://doi.org/10.1002/hep.32115Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/187980Test

المساهمون: Xianyong Yin, Kwangwoo Kim, Hiroyuki Suetsugu, So-Young Bang, Leilei Wen, Masaru Koido, Eunji Ha, Lu Liu, Yuma Sakamoto, Sungsin Jo, Rui-Xue Leng, Nao Otomo, Viktoryia Laurynenka, Young-Chang Kwon, Yujun Sheng, Nobuhiko Sugano, Mi Yeong Hwang, Weiran Li, Masaya Mukai, Kyungheon Yoon, Minglong Cai, Kazuyoshi Ishigaki, Won Tae Chung, He Huang, Daisuke Takahashi, Shin-Seok Lee, Mengwei Wang, Kohei Karino, Seung-Cheol Shim, Xiaodong Zheng, Tomoya Miyamura, Young Mo Kang, Dongqing Ye, Junichi Nakamura, Chang-Hee Suh, Yuanjia Tang, Goro Motomura, Yong-Beom Park, Huihua Ding, Takeshi Kuroda, Jung-Yoon Choe, Chengxu Li, Hiroaki Niiro, Youngho Park, Changbing Shen, Takeshi Miyamoto, Ga-Young Ahn, Wenmin Fei, Tsutomu Takeuchi, Jung-Min Shin, Keke Li, Yasushi Kawaguchi, Yeon-Kyung Lee, Yongfei Wang, Koichi Amano, Dae Jin Park, Wanling Yang, Yoshifumi Tada, Ken Yamaji, Masato Shimizu, Takashi Atsumi, Akari Suzuki, Takayuki Sumida, Yukinori Okada, Koichi Matsuda, Keitaro Matsuo, Yuta Kochi, Leah C Kottyan, Matthew T Weirauch, Sreeja Parameswaran, Shruti Eswar, Hanan Salim, Xiaoting Chen, Kazuhiko Yamamoto, John B Harley, Koichiro Ohmura, Tae-Hwan Kim, Sen Yang, Takuaki Yamamoto, Bong-Jo Kim, Nan Shen, Shiro Ikegawa, Hye-Soon Lee, Xuejun Zhang, Chikashi Terao, Yong Cui, Sang-Cheol Bae, Park, Yong Beom

مصطلحات موضوعية: Adult, Asians / genetics, Bayes Theorem, Case-Control Studies, China / epidemiology, China / ethnology, Far East / ethnology, Female, Genetic Loci / genetics, Genetic Predisposition to Disease / epidemiology, Genetic Predisposition to Disease / ethnology, Genetic Variation, Genome-Wide Association Study, Genotype, Humans, Japan / epidemiology, Japan / ethnology, Lupus Erythematosus, Systemic / epidemiology, Systemic / ethnology, Systemic / genetics, Male, Middle Aged, Prevalence, Republic of Korea / epidemiology, Republic of Korea / ethnology, epidemiology, genetic, polymorphism, systemic

العلاقة: ANNALS OF THE RHEUMATIC DISEASES; J00182; OAK-2022-04188; https://ir.ymlib.yonsei.ac.kr/handle/22282913/190414Test; T202126029; ANNALS OF THE RHEUMATIC DISEASES, Vol.80(5) : 632-640, 2021-05

الإتاحة: https://doi.org/10.1136/annrheumdis-2020-219209Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/190414Test

المؤلفون: Schneider, Susanne A., Hizli, Baccara, Alcalay, Roy N.

المصدر: http://lobid.org/resources/99370674841006441Test#!, 17(4):1378-1392.

مصطلحات موضوعية: TORC1 inhibitor, Deep Brain Stimulation/trends [MeSH], SNCA, GBA, Genetic Parkinson’s disease, Deep Brain Stimulation/methods [MeSH], alpha-Synuclein/genetics [MeSH], clinical trial, Parkinsonian Disorders/therapy [MeSH], Genetic Predisposition to Disease/genetics [MeSH], small molecule compounds, Mutation/genetics [MeSH], Genetic Predisposition to Disease/epidemiology [MeSH], Humans [MeSH], Precision Medicine/methods [MeSH], kinase inhibitor, ambroxol, Genetic Therapy/trends [MeSH], Precision Medicine/trends [MeSH], Leucine-Rich Repeat Serine-Threonine Protein Kinase-2/genetics [MeSH], Clinical Trials as Topic/methods [MeSH], Parkinsonian Disorders/genetics [MeSH], Parkinsonian Disorders/epidemiology [MeSH], Review, Genetic Therapy/methods [MeSH], LRRK2, Venglustat

العلاقة: https://repository.publisso.de/resource/frl:6471320Test; https://doi.org/10.1007/s13311-020-00920-8Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7483040Test/

الإتاحة: https://doi.org/10.1007/s13311-020-00920-8Test
https://repository.publisso.de/resource/frl:6471320Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7483040Test/

المؤلفون: Panousis, Nikolaos, Bertsias, George K, Ongen, Halit, Gergianaki, Irini, Tektonidou, Maria G, Trachana, Maria, Romano, Luciana, Bielser, Deborah, Howald, Cédric, Pamfil, Cristina, Fanouriakis, Antonis, Kosmara, Despoina, Repa, Argyro, Sidiropoulos, Prodromos, Dermitzakis, Emmanouil, Boumpas, Dimitrios T

المصدر: ISSN: 0003-4967 ; Annals of the Rheumatic Diseases, vol. 78, no. 8 (2019) p. 1079-1089.

مصطلحات موضوعية: info:eu-repo/classification/ddc/576.5, info:eu-repo/classification/ddc/590, Adult, Case-Control Studies, Disease Progression, Female, Gene Expression Profiling/methods, Genetic Predisposition to Disease/epidemiology, Genetic Variation, Genome-Wide Association Study, Genotype, Humans, Interferon Type I/genetics, Lupus Erythematosus, Systemic/genetics/immunology, Male, Middle Aged, Phenotype, RNA, Messenger/genetics, Reference Values, Transcriptome/genetics, Young Adult

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31167757; info:eu-repo/semantics/dataset/url/https://www.ebi.ac.uk/ega/studies/EGAS00001003662Test; info:eu-repo/grantAgreement/EC/H2020/742390/EU/PRECISION CARE IN SYSTEMIC AUTOIMMUNITY: AN INTEGRATED MULTI-TISSUE/LEVEL APPROACH FOR SYSTEMIC LUPUS ERYTHEMATOSUS (SLE)/LUPUSCARE; info:eu-repo/grantAgreement/EC/H2020/733100/EU/A Systems medicine approach to chronic inflammatory disease/SYSCID; https://archive-ouverte.unige.ch/unige:144675Test; unige:144675

الإتاحة: https://doi.org/10.1136/annrheumdis-2018-214379Test
https://archive-ouverte.unige.ch/unige:144675Test

المؤلفون: Høxbroe Michaelsen, Sanne, Ornstrup, Marie Juul, Poulsen, Morten Møller, Bennedbæk, Finn Noe, Gaustadnes, Mette, Rossing, Maria, Darling, Peter, Vestergaard, Peter, Mathiesen, Jes Sloth

المصدر: Høxbroe Michaelsen , S , Ornstrup , M J , Poulsen , M M , Bennedbæk , F N , Gaustadnes , M , Rossing , M , Darling , P , Vestergaard , P & Mathiesen , J S 2019 , ' Long-term follow-up of RET Y791F carriers in Denmark 1994-2017 : A National Cohort Study ' , Journal of Surgical Oncology , vol. 119 , no. 6 , pp. 687-693 . https://doi.org/10.1002/jso.25371Test

مصطلحات موضوعية: Adolescent, Adult, Aged, 80 and over, Carcinoma, Medullary/genetics, Child, Cohort Studies, Denmark/epidemiology, Follow-Up Studies, Genetic Predisposition to Disease/epidemiology, Heterozygote, Humans, Middle Aged, Multiple Endocrine Neoplasia Type 2a/genetics, Mutation, Pheochromocytoma/genetics, Proto-Oncogene Proteins c-ret/genetics, Thyroid Neoplasms/genetics, Young Adult

وصف الملف: application/pdf

الإتاحة: https://doi.org/10.1002/jso.25371Test
https://curis.ku.dk/portal/da/publications/longterm-followup-of-ret-y791f-carriers-in-denmark-19942017Test(5cd5c8c7-2c39-49df-b9e2-03ee91318308).html
https://curis.ku.dk/ws/files/251035315/Long_term_follow_up_of_RET_Y791F_carriers_in_Denmark_1994_2017_A_National_Cohort_Study_accepted_version_.pdfTest

المؤلفون: Feitosa, M.F., Kraja, A.T., Chasman, D.I., Sung, Y.J., Winkler, T.W., Ntalla, I., Guo, X., Franceschini, N., Cheng, C.Y., Sim, X., Vojinovic, D., Marten, J., Musani, S.K., Li, C., Bentley, A.R., Brown, M.R., Schwander, K., Richard, M.A., Noordam, R., Aschard, H., Bartz, T.M., Bielak, L.F., Dorajoo, R., Fisher, V., Hartwig, F.P., Horimoto, ARVR, Lohman, K.K., Manning, A.K., Rankinen, T., Smith, A.V., Tajuddin, S.M., Wojczynski, M.K., Alver, M., Boissel, M., Cai, Q., Campbell, A., Chai, J.F., Chen, X., Divers, J., Gao, C., Goel, A., Hagemeijer, Y., Harris, S.E., He, M., Hsu, F.C., Jackson, A.U., Kähönen, M., Kasturiratne, A., Komulainen, P., Kühnel, B., Laguzzi, F., Luan, J., Matoba, N., Nolte, I.M., Padmanabhan, S., Riaz, M., Rueedi, R., Robino, A., Said, M.A., Scott, R.A., Sofer, T., Stančáková, A., Takeuchi, F., Tayo, B.O., van der Most, P.J., Varga, T.V., Vitart, V., Wang, Y., Ware, E.B., Warren, H.R., Weiss, S., Wen, W., Yanek, L.R., Zhang, W., Zhao, J.H., Afaq, S., Amin, N., Amini, M., Arking, D.E., Aung, T., Boerwinkle, E., Borecki, I., Broeckel, U., Brown, M., Brumat, M., Burke, G.L., Canouil, M., Chakravarti, A., Charumathi, S., Ida Chen, Y.D., Connell, J.M., Correa, A., de Las Fuentes, L., de Mutsert, R., de Silva, H.J., Deng, X., Ding, J., Duan, Q., Eaton, C.B., Ehret, G., Eppinga, R.N., Evangelou, E., Faul, J.D., Felix, S.B., Forouhi, N.G., Forrester, T., Franco, O.H., Friedlander, Y., Gandin, I., Gao, H., Ghanbari, M., Gigante, B., Gu, C.C., Gu, D., Hagenaars, S.P., Hallmans, G., Harris, T.B., He, J., Heikkinen, S., Heng, C.K., Hirata, M., Howard, B.V., Ikram, M.A., John, U., Katsuya, T., Khor, C.C., Kilpeläinen, T.O., Koh, W.P., Krieger, J.E., Kritchevsky, S.B., Kubo, M., Kuusisto, J., Lakka, T.A., Langefeld, C.D., Langenberg, C., Launer, L.J., Lehne, B., Lewis, C.E., Li, Y., Lin, S., Liu, J., Loh, M., Louie, T., Mägi, R., McKenzie, C.A., Meitinger, T., Metspalu, A., Milaneschi, Y., Milani, L., Mohlke, K.L., Momozawa, Y., Nalls, M.A., Nelson, C.P., Sotoodehnia, N., Norris, J.M., O'Connell, J.R., Palmer, N.D., Perls, T., Pedersen, N.L., Peters, A., Peyser, P.A., Poulter, N., Raffel, L.J., Raitakari, O.T., Roll, K., Rose, L.M., Rosendaal, F.R., Rotter, J.I., Schmidt, C.O., Schreiner, P.J., Schupf, N., Scott, W.R., Sever, P.S., Shi, Y., Sidney, S., Sims, M., Sitlani, C.M., Smith, J.A., Snieder, H., Starr, J.M., Strauch, K., Stringham, H.M., Tan, NYQ, Tang, H., Taylor, K.D., Teo, Y.Y., Tham, Y.C., Turner, S.T., Uitterlinden, A.G., Vollenweider, P., Waldenberger, M., Wang, L., Wang, Y.X., Wei, W.B., Williams, C., Yao, J., Yu, C., Yuan, J.M., Zhao, W., Zonderman, A.B., Becker, D.M., Boehnke, M., Bowden, D.W., Chambers, J.C., Deary, I.J., Esko, T., Farrall, M., Franks, P.W., Freedman, B.I., Froguel, P., Gasparini, P., Gieger, C., Jonas, J.B., Kamatani, Y., Kato, N., Kooner, J.S., Kutalik, Z., Laakso, M., Laurie, C.C., Leander, K., Lehtimäki, T., Study, L.C., Magnusson, PKE, Oldehinkel, A.J., Penninx, BWJH, Polasek, O., Porteous, D.J., Rauramaa, R., Samani, N.J., Scott, J., Shu, X.O., van der Harst, P., Wagenknecht, L.E., Wareham, N.J., Watkins, H., Weir, D.R., Wickremasinghe, A.R., Wu, T., Zheng, W., Bouchard, C., Christensen, K., Evans, M.K., Gudnason, V., Horta, B.L., Kardia, SLR, Liu, Y., Pereira, A.C., Psaty, B.M., Ridker, P.M., van Dam, R.M., Gauderman, W.J., Zhu, X., Mook-Kanamori, D.O., Fornage, M., Rotimi, C.N., Cupples, L.A., Kelly, T.N., Fox, E.R., Hayward, C., van Duijn, C.M., Tai, E.S., Wong, T.Y., Kooperberg, C., Palmas, W., Rice, K., Morrison, A.C., Elliott, P., Caulfield, M.J., Munroe, P.B., Rao, D.C., Province, M.A., Levy, D.

المساهمون: InterAct Consortium

المصدر: PloS one, vol. 13, no. 6, pp. e0198166

مصطلحات موضوعية: Adolescent, Adult, Aged, 80 and over, Alcohol Drinking/epidemiology, Alcohol Drinking/genetics, Blood Pressure/genetics, Cohort Studies, Continental Population Groups/genetics, Continental Population Groups/statistics & numerical data, Female, Gene-Environment Interaction, Genetic Predisposition to Disease/epidemiology, Genetic Predisposition to Disease/genetics, Genome-Wide Association Study, Humans, Hypertension/epidemiology, Hypertension/genetics, Male, Middle Aged, Pedigree, Polymorphism, Single Nucleotide, Young Adult

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29912962; info:eu-repo/semantics/altIdentifier/eissn/1932-6203; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_FC7DB3103C3C5; https://serval.unil.ch/notice/serval:BIB_FC7DB3103C3CTest; urn:issn:1932-6203; https://serval.unil.ch/resource/serval:BIB_FC7DB3103C3C.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_FC7DB3103C3C5Test

الإتاحة: https://doi.org/10.1371/journal.pone.0198166Test
https://serval.unil.ch/notice/serval:BIB_FC7DB3103C3CTest
https://serval.unil.ch/resource/serval:BIB_FC7DB3103C3C.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_FC7DB3103C3C5Test

المؤلفون: Sanford Biggerstaff, Julie

المساهمون: Idaho Cytogenetics Diagnostic Laboratory, Boise, ID 83706, USA

مصطلحات موضوعية: Chromosome 4, chromosome 9, translocation, SEC31A, JAK2, Hodgkin Lymphoma, Leukaemia Section, Adult, Aged, 80 and over, Animals, Bone Marrow Transplantation, Chromosomes, Human, Pair 4, Pair 9, Disease Models, Animal, Female, Gene Rearrangement/*genetics, Genetic Predisposition to Disease/epidemiology, HEK293 Cells, Hodgkin Disease/epidemiology/*genetics, Humans, Janus Kinase 2/*genetics

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/t0409q21p24ID1682.htmlTest; Julie, Sanford Biggerstaff. t(4;9)(q21.22;p24) SEC31A/JAK2. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2018, 5, p. 216-217; http://hdl.handle.net/2042/68905Test; https://doi.org/10.4267/2042/68905Test

الإتاحة: https://doi.org/10.4267/2042/68905Test
http://hdl.handle.net/2042/68905Test

المؤلفون: Jones, Gregory T, Tromp, Gerard, Kuivaniemi, Helena, Gretarsdottir, Solveig, Baas, Annette F, Giusti, Betti, Strauss, Ewa, van 't Hof, Femke N, Webb, Thomas, Erdman, Robert, Ritchie, Marylyn D, Elmore, James R, Verma, Anurag, Pendergrass, Sarah, Kullo, Iftikhar J, Ye, Zi, Peissig, Peggy L, Gottesman, Omri, Verma, Shefali S, Malinowski, Jennifer, Rasmussen-Torvik, Laura J, Borthwick, Kenneth, Smelser, Diane T, Crosslin, David R, de Andrade, Mariza, Ryer, Evan J, McCarty, Catherine A, Bottinger, Erwin P, Pacheco, Jennifer A, Crawford, Dana C, Carrell, David S, Gerhard, Glenn S, Franklin, David P, Carey, David J, Phillips, Victoria L, Williams, Michael J, Wei, Wenhua, Blair, Ross, Hill, Andrew A, Vasudevan, Thodur M, Lewis, David R, Thomson, Ian A, Krysa, Jo, Hill, Geraldine B, Roake, Justin, Merriman, Tony R, Oszkinis, Grzegorz, Galora, Silvia, Saracini, Claudia, Abbate, Rosanna, Pulli, Raffaele, Pratesi, Carlo, Saratzis, Athanasios, Verissimo, Anna, Bumpstead, Suzannah J, Badger, Stephen A, Clough, Rachel E, Cockerill, Gillian W, Hafez, Hany, Scott, D J, Futers, T S, Romaine, Simon P, Bridge, Katherine, Griffin, Kathryn J, Bailey, Marc A, Smith, Alberto, Thompson, Matt M, van Bockxmeer, Frank, Matthiasson, Stefan E, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Blankensteijn, Jan D, Teijink, Joep A, Wijmenga, Cisca, de Graaf, Jacqueline, Kiemeney, Lambertus A, Lindholt, Jes S, Hughes, Anne E, Bradley, Declan T, Stirrups, Kathleen, Golledge, Jonathan, Norman, Paul E, Powell, Janet T, Humphries, Steve E, Hamby, Stephen E, Goodall, Alison H, Nelson, Christopher P, Sakalihasan, Natzi, Courtois, Audrey, Ferrell, Robert E, Eriksson, Per, Folkersen, Lasse, Franco-Cereceda, Anders, Eicher, John D, Johnson, Andrew D, Betsholtz, Christer, Ruusalepp, Arno, Franzén, Oscar, Schadt, Eric, Björkegren, Johan L, Lipovich, Leonard, Drolet, Anne M, Verhoeven, Eric, Zeebregts, Clark J, Geelkerken, Robert H, van Sambeek, Marc R, van Sterkenburg, Steven M, de Vries, Jean-Paul P, Stefansson, Kari, Thompson, John R, de Bakker, Paul I, Deloukas, Panos, Sayers, Robert D, Harrison, Seamus, van Rij, Andre M, Samani, Nilesh J, Bown, Matthew J

المصدر: Jones , G T , Tromp , G , Kuivaniemi , H , Gretarsdottir , S , Baas , A F , Giusti , B , Strauss , E , van 't Hof , F N , Webb , T , Erdman , R , Ritchie , M D , Elmore , J R , Verma , A , Pendergrass , S , Kullo , I J , Ye , Z , Peissig , P L , Gottesman , O , Verma , S S , Malinowski , J , Rasmussen-Torvik , L J , Borthwick , K , ....

مصطلحات موضوعية: aortic aneurysm abdominal, computational biology, genetics, genome-wide association study, matrix metalloproteinases, meta-analysis, Aortic Aneurysm, Abdominal/diagnosis, Genetic Predisposition to Disease/epidemiology, Genome-Wide Association Study/methods, Humans, Genetic Loci/genetics, Genetic Variation/genetics

وصف الملف: application/pdf

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/19d22780-ee83-4f1f-8a4d-5be341f66f2dTest

الإتاحة: https://doi.org/10.1161/CIRCRESAHA.116.308765Test
https://portal.findresearcher.sdu.dk/da/publications/19d22780-ee83-4f1f-8a4d-5be341f66f2dTest
https://findresearcher.sdu.dk/ws/files/124389378/Meta_Analysis_of_Genome_Wide_Association_Studies_for_Abdominal_Aortic_Aneurysm_Identifies_Four_New_Disease_Specific_Risk_Loci.pdfTest

المؤلفون: Bürger, Katharina, Arzberger, T., Stephan, J., Levin, J., Edbauer, D.

المصدر: Der Nervenarzt 88(2), 163-172 (2017). doi:10.1007/s00115-016-0259-x

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Aged, Female, Frontotemporal Lobar Degeneration: diagnosis, Frontotemporal Lobar Degeneration: epidemiology, Frontotemporal Lobar Degeneration: genetics, Genetic Predisposition to Disease: epidemiology, Genetic Predisposition to Disease: genetics, Germany: epidemiology, Humans, Male, Mutation: genetics, Nerve Tissue Proteins: genetics, Polymorphism, Single Nucleotide: genetics, Prevalence, Risk Factors, Nerve Tissue Proteins

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/1433-0407; info:eu-repo/semantics/altIdentifier/pmid/pmid:27999880; info:eu-repo/semantics/altIdentifier/issn/0028-2804; https://pub.dzne.de/record/139051Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-05373%22Test

الإتاحة: https://doi.org/10.1007/s00115-016-0259-xTest
https://pub.dzne.de/record/139051Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-05373%22Test