المؤلفون: Madireddy, Lohith, Patsopoulos, Niklaos A, Cotsapas, Chris, Bos, Steffan D, Beecham, Ashley, McCauley, Jacob, Kim, Kicheol, Jia, Xiaoming, Santaniello, Adam, Caillier, Stacy J, Andlauer, Till FM, Barcellos, Lisa F, Berge, Tone, Bernardinelli, Luisa, Martinelli-Boneschi, Filippo, Booth, David R, Briggs, Farren, Celius, Elisabeth G, Comabella, Manuel, Comi, Giancarlo, Cree, Bruce AC, D'Alfonso, Sandra, Dedham, Katrina, Duquette, Pierre, Efthimios, Dardiotis, Esposito, Federica, Fontaine, Bertrand, Gasperi, Christiane, Goris, An, Dubois, Benedicte, Gourraud, Pierre-Antoine, Hadjigeorgiou, Georgios, Haines, Jonathan, Hawkins, Clive, Hemmer, Bernhard, Hintzen, Rogier, Horakova, Dana, Isobe, Noriko, Kalra, Seema, Kira, Jun-ichi, Khalil, Michael, Kockum, Ingrid, Lill, Christina M, Lincoln, Matthew R, Luessi, Felix, Martin, Roland, Oturai, Annette, Palotie, Aarno, Pericak-Vance, Margaret A, Henry, Roland, Saarela, Janna, Ivinson, Adrian, Olsson, Tomas, Taylor, Bruce V, Stewart, Graeme J, Harbo, Hanne F, Compston, Alastair, Hauser, Stephen L, Hafler, David A, Zipp, Frauke, De Jager, Philip, Sawcer, Stephen, Oksenberg, Jorge R, Baranzini, Sergio E

المصدر: Nature Communications. 10(1)

مصطلحات موضوعية: Human Genome, Autoimmune Disease, Multiple Sclerosis, Genetics, Biotechnology, Brain Disorders, Neurodegenerative, Clinical Research, Neurosciences, 2.1 Biological and endogenous factors, Aetiology, Inflammatory and immune system, Gene Expression Regulation, Genes, Regulator, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Polymorphism, Single Nucleotide, Systems Biology, International Multiple Sclerosis Genetics Consortium

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5f91v8cbTest

المؤلفون: Moutsianas, Loukas, Jostins, Luke, Beecham, Ashley, Dilthey, Alexander, Xifara, Dionysia, Ban, Maria, Shah, Tejas, Patsopoulos, Nikolaos, Alfredsson, Lars, Anderson, Carl, Attfield, Katherine, Barrett, Jeffrey, Binder, Thomas, Booth, David, Buck, Dorothea, Celius, Elisabeth, Cotsapas, Chris, DAlfonso, Sandra, Dendrou, Calliope, Donnelly, Peter, Dubois, Bénédicte, Fontaine, Bertrand, Fugger, Lars, Goris, An, Graetz, Christiane, Hemmer, Bernhard, Hillert, Jan, Kockum, Ingrid, Leslie, Stephen, Lill, Christina, Martinelli-Boneschi, Filippo, Olsson, Tomas, Oturai, Annette, Saarela, Janna, Søndergaard, Helle, Spurkland, Anne, Taylor, Bruce, Winkelmann, Juliane, Zipp, Frauke, Haines, Jonathan, Pericak-Vance, Margaret, Spencer, Chris, Stewart, Graeme, Hafler, David, Ivinson, Adrian, Harbo, Hanne, De Jager, Philip, Compston, Alastair, McCauley, Jacob, Sawcer, Stephen, McVean, Gil, Hauser, Stephen, Oksenberg, Jorge, Baranzini, Sergio, Gourraud, Pierre-Antoine

المصدر: Nature Genetics. 47(10)

مصطلحات موضوعية: Alleles, Epistasis, Genetic, Genetic Predisposition to Disease, Histocompatibility Antigens Class II, Humans, Multiple Sclerosis, Polymorphism, Single Nucleotide

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/01z6j930Test

المؤلفون: Goris, An, van Setten, Jessica, Diekstra, Frank, Ripke, Stephan, Patsopoulos, Nikolaos A, Sawcer, Stephen J, van Es, Michael, Andersen, Peter M, Melki, Judith, Meininger, Vincent, Hardiman, Orla, Landers, John E, Brown, Robert H, Shatunov, Aleksey, Leigh, Nigel, Al-Chalabi, Ammar, Shaw, Christopher E, Traynor, Bryan J, Chiò, Adriano, Restagno, Gabriella, Mora, Gabriele, Ophoff, Roel A, Oksenberg, Jorge R, Van Damme, Philip, Compston, Alastair, Robberecht, Wim, Dubois, Bénédicte, van den Berg, Leonard H, De Jager, Philip L, Veldink, Jan H, de Bakker, Paul IW

المصدر: Human Molecular Genetics. 23(7)

مصطلحات موضوعية: Human Genome, ALS, Multiple Sclerosis, Rare Diseases, Autoimmune Disease, Neurosciences, Genetics, Neurodegenerative, Clinical Research, Brain Disorders, 2.1 Biological and endogenous factors, Aetiology, Neurological, Amyotrophic Lateral Sclerosis, Comorbidity, Genetic Predisposition to Disease, Humans, Polymorphism, Single Nucleotide, International Multiple Sclerosis Genetics Consortium, Australia and New Zealand MS Genetics Consortium, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/84v7j6brTest

المؤلفون: Cree, Bruce AC, Rioux, John D, McCauley, Jacob L, Gourraud, Pierre-Antoine FD, Goyette, Philippe, McElroy, Joseph, De Jager, Philip, Santaniello, Adam, Vyse, Timothy J, Gregersen, Peter K, Mirel, Daniel, Hafler, David A, Haines, Jonathan L, Pericak-Vance, Margaret A, Compston, Alastair, Sawcer, Stephen J, Oksenberg, Jorge R, Hauser, Stephen L, IMAGEN, IMSGC

المصدر: PloS one. 5(6)

مصطلحات موضوعية: IMAGEN, IMSGC, Humans, Multiple Sclerosis, Genetic Predisposition to Disease, Histocompatibility Antigens Class I, HLA-DR Antigens, Logistic Models, Case-Control Studies, Haplotypes, Linkage Disequilibrium, Polymorphism, Single Nucleotide, HLA-DRB1 Chains, Polymorphism, Single Nucleotide, General Science & Technology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/7qv5493nTest

المؤلفون: Yeo, Tai Wai, De Jager, Philip L, Gregory, Simon G, Barcellos, Lisa F, Walton, Amie, Goris, An, Fenoglio, Chiara, Ban, Maria, Taylor, Craig J, Goodman, Reyna S, Walsh, Emily, Wolfish, Cara S, Horton, Roger, Traherne, James, Beck, Stephan, Trowsdale, John, Caillier, Stacy J, Ivinson, Adrian J, Green, Todd, Pobywajlo, Susan, Lander, Eric S, Pericak-Vance, Margaret A, Haines, Jonathan L, Daly, Mark J, Oksenberg, Jorge R, Hauser, Stephen L, Compston, Alastair, Hafler, David A, Rioux, John D, Sawcer, Stephen

المصدر: Annals of Neurology. 61(3)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Neurosciences, Clinical Sciences, Human Genome, Brain Disorders, Genetics, Autoimmune Disease, Multiple Sclerosis, Neurodegenerative, Aetiology, 2.1 Biological and endogenous factors, Inflammatory and immune system, Adult, Female, Genetic Predisposition to Disease, HLA-D Antigens, Humans, Major Histocompatibility Complex, Male, Microsatellite Repeats, Middle Aged, Polymorphism, Single Nucleotide, Neurology & Neurosurgery, Clinical sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/0z47v2mxTest

المؤلفون: Smets, Ide, Fiddes, Barnaby, Garcia-Perez, Josselyn E, He, Di, Mallants, Klara, Liao, Wenjia, Dooley, James, Wang, George, Humblet-Baron, Stephanie, Dubois, Bénédicte, Compston, Alastair, Jones, Joanne, Coles, Alasdair, Liston, Adrian, Ban, Maria, Goris, An, Sawcer, Stephen

مصطلحات موضوعية: B-Lymphocytes, B7-2 Antigen, CD40 Antigens, Correlation of Data, Cytokines, Female, Gene Expression Regulation, Genetic Predisposition to Disease, Genotype, Humans, Interleukin-10, Male, Multiple Sclerosis, Polymorphism, Single Nucleotide

وصف الملف: Print; application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

العلاقة: https://www.repository.cam.ac.uk/handle/1810/276186Test

الإتاحة: https://doi.org/10.17863/CAM.23468Test
https://www.repository.cam.ac.uk/handle/1810/276186Test

المؤلفون: Beecham, Ashley H., Patsopoulos, Nikolaos A., Xifara, Dionysia K., Davis, Mary F., Kemppinen, Anu, Cotsapas, Chris, Shah, Tejas S., Spencer, Chris, Booth, David, Goris, An, Oturai, Annette, Saarela, Janna, Fontaine, Bertrand, Hemmer, Bernhard, Martin, Claes, Zipp, Frauke, D'Alfonso, Sandra, F. MARTINELLI BONESCHI, Taylor, Bruce, Harbo, Hanne F., Kockum, Ingrid, Hillert, Jan, Olsson, Tomas, Ban, Maria, Oksenberg, Jorge R., Hintzen, Rogier, Barcellos, Lisa F., C. Agliardi, Alfredsson, Lars, Alizadeh, Mehdi, Anderson, Carl, Andrews, Robert, Sà ̧ndergaard, Helle Bach, Baker, Amie, Band, Gavin, Baranzini, Sergio E., Barizzone, Nadia, Barrett, Jeffrey, Bellenguez, Céline, Bergamaschi, Laura, Bernardinelli, Luisa, Berthele, Achim, Biberacher, Viola, Binder, Thomas M. C., Blackburn, Hannah, Bomfim, Izaura L., P.G. Brambilla, Broadley, Simon, Brochet, Bruno, Brundin, Lou, Buck, Dorothea, Butzkueven, Helmut, Caillier, Stacy J., Camu, William, Carpentier, Wassila, Cavalla, Paola, Celius, Elisabeth G., Coman, IrÃne, Comi, Giancarlo, Corrado, Lucia, Cosemans, Leentje, Cournu-Rebeix, Isabelle, Cree, Bruce A. C., D.M. Cusi, Damotte, Vincent, Defer, Gilles, Delgado, Silvia R., Deloukas, Panos, Di Sapio, Alessia, Dilthey, Alexander T., Donnelly, Peter, Dubois, Bénédicte, Duddy, Martin, Edkins, Sarah, Elovaara, Irina, Esposito, Federica, Evangelou, Nikos, Fiddes, Barnaby, Field, Judith, Franke, Andre, Freeman, Colin, Frohlich, Irene Y., D. Galimberti, Gieger, Christian, Gourraud, Pierre-Antoine, Graetz, Christiane, Graham, Andrew, Grummel, Verena, Guaschino, Clara, Hadjixenofontos, Athena, Hakonarson, Hakon, Halfpenny, Christopher, Hall, Gillian, Hall, Per, Hamsten, Anders, Harley, James, Harrower, Timothy, Hawkins, Clive, Hellenthal, Garrett, Hillier, Charles, Hobart, Jeremy, Hoshi, Muni, Hunt, Sarah E., Jagodic, Maja, Jelcic, Ilijas, Jochim, Angela, Kendall, Brian, Kermode, Allan, Kilpatrick, Trevor, Koivisto, Keijo, Konidari, Ioanna, Korn, Thomas, Kronsbein, Helena, Langford, Cordelia, Larsson, Malin, Lathrop, Mark, Lebrun-Frenay, Christine, Lechner-Scott, Jeannette, Lee, Michelle H., Leone, Maurizio A., Leppä, Virpi, Liberatore, Giuseppe, Lie, Benedicte A., Lill, Christina M., Lindén, Magdalena, Link, Jenny, Luessi, Felix, Lycke, Jan, F. Macciardi, Männistö, Satu, Manrique, Clara P., Martin, Roland, Martinelli, Vittorio, Mason, Deborah, Mazibrada, Gordon, McCabe, Cristin, Mero, Inger-Lise, Mescheriakova, Julia, Moutsianas, Loukas, Myhr, Kjell-Morten, Nagels, Guy, Nicholas, Richard, Nilsson, Petra, Piehl, Fredrik, Pirinen, Matti, Price, Siân E., Quach, Hong, Reunanen, Mauri, Robberecht, Wim, Robertson, Neil P., Rodegher, Mariaemma, Rog, David, Salvetti, Marco, Schnetz-Boutaud, Nathalie C., Sellebjerg, Finn, Selter, Rebecca C., Schaefer, Catherine, Shaunak, Sandip, Shen, Ling, Shields, Simon, Siffrin, Volker, Slee, Mark, Sorensen, Per Soelberg, Sorosina, Melissa, Sospedra, Mireia, Spurkland, Anne, Strange, Amy, Sundqvist, Emilie, Thijs, Vincent, Thorpe, John, Ticca, Anna, Tienari, Pentti, Van Duijn, Cornelia, Visser, Elizabeth M., Vucic, Steve, Westerlind, Helga, Wiley, James S., Wilkins, Alastair, Wilson, James F., Winkelmann, Juliane, Zajicek, John, Zindler, Eva, Haines, Jonathan L., Pericak-Vance, Margaret A., Ivinson, Adrian J., Stewart, Graeme, Hafler, David, Hauser, Stephen L., Compston, Alastair, McVean, Gil, De Jager, Philip, Sawcer, Stephen J., McCauley, Jacob L.

المساهمون: B. Ashley H., P. Nikolaos A., X. Dionysia K., D. Mary F., K. Anu, C. Chri, S. Tejas S., S. Chri, B. David, G. An, O. Annette, S. Janna, F. Bertrand, H. Bernhard, M. Clae, Z. Frauke, D. Sandra, F. MARTINELLI BONESCHI, T. Bruce, H. Hanne F., K. Ingrid, H. Jan, O. Toma, B. Maria, O. Jorge R., H. Rogier, B. Lisa F., C. Agliardi, A. Lar, A. Mehdi, A. Carl, A. Robert, S. Helle Bach, B. Amie, B. Gavin, B. Sergio E., B. Nadia, B. Jeffrey, B. Cã©line, B. Laura, B. Luisa, B. Achim, B. Viola, B. Thomas M. C., B. Hannah, B. Izaura L., P.G. Brambilla, B. Simon, B. Bruno, B. Lou, B. Dorothea, B. Helmut, C. Stacy J., C. William, C. Wassila, C. Paola, C. Elisabeth G., C. Irãne, C. Giancarlo, C. Lucia, C. Leentje, C. Isabelle, C. Bruce A. C., D.M. Cusi, D. Vincent, D. Gille, D. Silvia R., D. Pano, D.S. Alessia, D. Alexander T., D. Peter, D. Bã©nã©dicte, D. Martin, E. Sarah, E. Irina, E. Federica, E. Niko, F. Barnaby, F. Judith, F. Andre, F. Colin, F. Irene Y., D. Galimberti, G. Christian, G. Pierre-Antoine, G. Christiane, G. Andrew, G. Verena, G. Clara, H. Athena, H. Hakon, H. Christopher, H. Gillian, H. Per, H. Ander, H. Jame, H. Timothy, H. Clive, H. Garrett, H. Charle

مصطلحات موضوعية: Chromosome Mapping, European Continental Ancestry Group, Gene Frequency, Genetic Loci, Genetic Predisposition to Disease, Genetic Variation, Genome-Wide Association Study, Genotype, Human, Multiple Sclerosi, Polymorphism, Single Nucleotide, Genetics, Settore MED/26 - Neurologia, Settore MED/14 - Nefrologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/24076602; info:eu-repo/semantics/altIdentifier/wos/WOS:000326384100016; volume:45; issue:11; firstpage:1353; lastpage:1360; numberofpages:8; journal:NATURE GENETICS; http://hdl.handle.net/2434/533429Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84887058596

الإتاحة: https://doi.org/10.1038/ng.2770Test
http://hdl.handle.net/2434/533429Test

المؤلفون: Goris, An, van Setten, Jessica, Diekstra, Frank, Ripke, Stephan, Patsopoulos, Nikolaos A., Sawcer, Stephen J., International Multiple Sclerosis Genetics Consortium, van Es M, Australia and New Zealand MS Genetics Consortium, van Es, Michael, Andersen, Peter M., Melki, Judith, Meininger, Vincent, Hardiman, Orla, Landers, John E., Brown, Robert H., Shatunov, Aleksey, Leigh, Nigel, Al-Chalabi, Ammar, Shaw, Christopher E., Traynor, Bryan J., Chió, Adriano, Restagno, Gabriella, Mora, Gabriele, Ophoff, Roel A., Oksenberg, Jorge R., Van Damme, Philip, Compston, Alastair, Robberecht, Wim, Dubois, Bénédicte, van den Berg, Leonard H., De Jager, Philip L., Veldink, Jan H., de Bakker, Paul I. W. Collaborators: Barcellos L, Booth D, McCauley JL, Comabella M, Compston A, D'Alfonso S, De Jager P, Fontaine B, Goris A, Hafler D, Haines J, Harbo HF, Hauser SL, Hawkins C, Hemmer B, Hillert J, Ivinson A, Kockum I, Martin R, F. Martinelli Boneschi, Oksenberg J, Olsson T, Oturai A, Patsopoulos N, Pericak-Vance M, Saarela J, Sawcer S, Spurkland A, Stewart G, Zipp F, Scott RJ, Lechner-Scott J, Moscato P, Booth DR, Stewart GJ, Heard RN, Mason D, Griffiths L, Broadley S, Brown MA, Slee M, Foote SJ, Stankovich J, Taylor BV, Wiley J, Bahlo M, Perreau V, Field J, Butzkueven H, Kilpatrick TJ, Rubio J, Marriott M, Carroll WM, Kermode A.G.

المساهمون: A. Gori, J. van Setten, F. Diekstra, S. Ripke, N.A. Patsopoulo, S.J. Sawcer, V.E.M. International Multiple Sclerosis Genetics Consortium, Australia and New Zealand MS Genetics Consortium, E. Van, Michael, P.M. Andersen, J. Melki, V. Meininger, O. Hardiman, J.E. Lander, R.H. Brown, A. Shatunov, N. Leigh, A. Al-Chalabi, C.E. Shaw, B.J. Traynor, A. Chiã³, G. Restagno, G. Mora, R.A. Ophoff, J.R. Oksenberg, P. Van Damme, A. Compston, W. Robberecht, B. Duboi, L.H. van den Berg, P.L. De Jager, J.H. Veldink, D. Bakker, P.I.W. Collaborators: Barcellos L, D. Booth, J. Mccauley, M. Comabella, S. D'Alfonso, P. De Jager, B. Fontaine, D. Hafler, J. Haine, H. Harbo, S. Hauser, C. Hawkin, B. Hemmer, J. Hillert, A. Ivinson, I. Kockum, R. Martin, F. Martinelli Boneschi, J. Oksenberg, T. Olsson, A. Oturai, N. Patsopoulo, M. Pericak-Vance, J. Saarela, S. Sawcer, A. Spurkland, G. Stewart, F. Zipp, R. Scott, J. Lechner-Scott, P. Moscato, R. Heard, D. Mason, L. Griffith, S. Broadley, M. Brown, M. Slee, S. Foote, J. Stankovich, B. Taylor, J. Wiley, M. Bahlo, V. Perreau, J. Field, H. Butzkueven, T. Kilpatrick, J. Rubio, M. Marriott, W. Carroll, A.G. Kermode

مصطلحات موضوعية: Amyotrophic Lateral Sclerosi, Comorbidity, Genetic Predisposition to Disease, Human, Multiple Sclerosi, Polymorphism, Single Nucleotide, Molecular Biology, Genetic, Genetics (clinical), Settore MED/26 - Neurologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/24234648; info:eu-repo/semantics/altIdentifier/wos/WOS:000333267900020; volume:23; issue:7; firstpage:1916; lastpage:1922; numberofpages:7; journal:HUMAN MOLECULAR GENETICS; http://hdl.handle.net/2434/533508Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84902540564; http://hmg.oxfordjournals.orgTest/

الإتاحة: https://doi.org/10.1093/hmg/ddt574Test
http://hdl.handle.net/2434/533508Test
http://hmg.oxfordjournals.orgTest/

المؤلفون: Maller, Julian B., McVean, Gilean, Byrnes, Jake, Vukcevic, Damjan, Palin, Kimmo, Su, Zhan, Howson, Joanna M M, Auton, Adam, Myers, Simon, Morris, Andrew, Pirinen, Matti, Brown, Matthew A., Burton, Paul R., Caulfield, Mark J., Compston, Alastair, Farrall, Martin, Hall, Alistair S., Hattersley, Andrew T., Hill, Adrian V S, Mathew, Christopher G., Pembrey, Marcus, Satsangi, Jack, Stratton, Michael R., Worthington, Jane, Craddock, Nick, Hurles, Matthew, Ouwehand, Willem, Parkes, Miles, Rahman, Nazneen, Duncanson, Audrey, Todd, John A., Kwiatkowski, Dominic P., Samani, Nilesh J., Gough, Stephen C L, McCarthy, Mark I., Deloukas, Panagiotis, Donnelly, Peter

المصدر: Maller , J B , McVean , G , Byrnes , J , Vukcevic , D , Palin , K , Su , Z , Howson , J M M , Auton , A , Myers , S , Morris , A , Pirinen , M , Brown , M A , Burton , P R , Caulfield , M J , Compston , A , Farrall , M , Hall , A S , Hattersley , A T , Hill , A V S , Mathew , C G , Pembrey , M , Satsangi , J , ....

مصطلحات موضوعية: Bayes Theorem, CTLA-4 Antigen, Coronary Artery Disease, Cyclin-Dependent Kinase 5, Cyclin-Dependent Kinase Inhibitor p15, Diabetes Mellitus, Type 2, Genes, p16, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Graves Disease, Homeodomain Proteins, Humans, Polymorphism, Single Nucleotide, Proteins, Transcription Factor 7-Like 2 Protein, Transcription Factors

العلاقة: https://research-information.bris.ac.uk/en/publications/c07c3006-ff14-48d9-a1df-9bb5cc0fda32Test

الإتاحة: https://doi.org/10.1038/ng.2435Test
https://hdl.handle.net/1983/c07c3006-ff14-48d9-a1df-9bb5cc0fda32Test
https://research-information.bris.ac.uk/en/publications/c07c3006-ff14-48d9-a1df-9bb5cc0fda32Test
http://www.scopus.com/inward/record.url?scp=84870502629&partnerID=8YFLogxKTest

المؤلفون: The International Multiple Sclerosis Genetics Consortium, Leppä, Virpi, Suraka, Ida, Tienari, Pentti, Elovaara, Irina, Compston, Alastair, Sawcer, Stephen, Robertson, Neil, De Jager, Philip, Aubin, Cristin, Hafler, David, Bang Oturai, Annette, Bach Sondergaard, Helle, Sellebjerg, Finn, SoelbergSorensen, Per, Hemmer, Bernhard, Cepok, Sabine, Winkelmann, Juliane, Wichmann, Heinz-Eric, Comabella, Manuel, Bustamante, Marta, Montalban, Xavier, Olsson, Tomas, Kockum, Ingrid, Hillert, Jan, Alfredsson, Lars, Goris, An, Dubois, Bénédicte, Mero, Inger-Lise, Smestad, Cathrine, Celius, Elisabeth, Harbo, Hanne, D'Alfonso, Sandra, Bergamaschi, Laura, Maurizio, Leone, Ristori, Giovanni, Kappos, Ludwig, Hauser, Stephen, Cournu-Rebeix, Isabelle, Fontaine, Bertrand, Boonen, Steven, Polman, Chris, Palotie, Arnoo, Peltonen, Leena, Saarela, Janna

مصطلحات موضوعية: Antigens, CD, Differentiation, T-Lymphocyte, Case-Control Studies, Humans, Interferon Regulatory Factors, Multiple Sclerosis, Polymorphism, Single Nucleotide, Receptors, Tumor Necrosis Factor, Type I

العلاقة: PLoS One vol:6 issue:4; https://lirias.kuleuven.be/handle/123456789/314810Test; http://dx.plos.org/10.1371/journal.pone.0018813Test

الإتاحة: https://doi.org/10.1371/journal.pone.0018813Test
https://lirias.kuleuven.be/handle/123456789/314810Test