المؤلفون: Zhu-Wen Yi, Qing-Nan He, Ying Wang, Xiqiang Dang, Yongzhen Li, Haibo Liu

المصدر: BMC Nephrology
BMC Nephrology, Vol 21, Iss 1, Pp 1-5 (2020)

مصطلحات موضوعية: Nephrology, Male, medicine.medical_specialty, Gout, 030232 urology & nephrology, Mutation, Missense, Mothers, Case Report, Hyperuricemia, 030204 cardiovascular system & hematology, lcsh:RC870-923, Kidney, UMOD, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Uromodulin, medicine, Missense mutation, Humans, Family history, Child, Genetic testing, Genetics, medicine.diagnostic_test, ADTKD, business.industry, Arthritis, Siblings, Kidney disease, lcsh:Diseases of the genitourinary system. Urology, medicine.disease, HNF1B, Nephritis, Interstitial, Allelic heterogeneity, Female, business, Hyperuricaemia

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09261b213347e5ab98c937a6b2c7eae9Test
http://europepmc.org/articles/PMC7449067Test

المؤلفون: Lotte Jacobs, Xabier L. Aranguren, Paolo Manunta, Giulia Coppiello, Zhenyu Zhang, Nicholas Cauwenberghs, Lutgarde Thijs, Daniele Cusi, Aernout Luttun, Cristina Barlassina, Matteo Barcella, Fang Fei Wei, Jan A. Staessen, Peter Verhamme, Wen-Yi Yang, Erika Salvi, Thibault Petit, Tatiana Kuznetsova, Judita Knez, Simona Delli Carpini, Lorena Citterio, Yu Mei Gu, Azusa Hara

المساهمون: Epidemiologie, RS: CARIM - R3 - Vascular biology, Yang, Wy, Petit, T, Thijs, L, Zhang, Zy, Jacobs, L, Hara, A, Wei, Ff, Salvi, E, Citterio, L, DELLI CARPINII, S, Gu, Ym, Knez, J, Cauwenberghs, N, Barcella, M, Barlassina, C, Manunta, Paolo, Coppiello, G, Aranguren, Xl, Kuznetsova, T, Cusi, D, Verhamme, P, Luttun, A, Staessen, Ja

المصدر: BMC Genetics
BMC Genetics, 16:116. BioMed Central

مصطلحات موضوعية: Adult, Male, Genotype, Population, Single-nucleotide polymorphism, Comorbidity, Coronary Artery Disease, Biology, Polymorphism, Single Nucleotide, Coronary artery disease, Young Adult, Belgium, Genetics, medicine, Basic Helix-Loop-Helix Transcription Factors, Ethnicity, Humans, Genetics(clinical), Myocardial infarction, Clinical genetics, education, Genetics (clinical), TCF15, Homeodomain Proteins, education.field_of_study, MEOX2, Incidence (epidemiology), Incidence, Hazard ratio, Haplotype, Genetic Variation, Translational research, Middle Aged, medicine.disease, Confidence interval, 3. Good health, Coronary heart disease, Haplotypes, Population science, Female, Research Article

وصف الملف: Electronic

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dde0281bd0d1a9db3d0597cd8a9cb16fTest
http://europepmc.org/articles/PMC4591634Test