دورية أكاديمية

Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity

التفاصيل البيبلوغرافية
العنوان: Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity
المؤلفون: Creemers, JWM, Choquet, H, Stijnen, P, Vatin, V, Pigeyre, M, Beckers, S, Meulemans, S, Than, ME, Yengo, L, Tauber, M, Balkan, B, Elliott, P, Jarvelin, M-R, Van Hul, W, Van Gaal, L, Horber, F, Pattou, F, Froguel, P, Meyre, D
المساهمون: Medical Research Council (MRC)
المصدر: 390 ; 383
بيانات النشر: American Diabetes Association
سنة النشر: 2011
المجموعة: Imperial College London: Spiral
مصطلحات موضوعية: Science & Technology, Life Sciences & Biomedicine, Endocrinology & Metabolism, BODY-MASS INDEX, GENOME-WIDE ASSOCIATION, EARLY-ONSET OBESITY, PROPROTEIN CONVERTASES, MISSENSE MUTATION, COMMON OBESITY, VARIANTS, RECEPTOR, GENE, SPECIFICITY, Adult, Female, Genotype, Glycosylation, Heterozygote, Humans, Male, Middle Aged, Mutation, Obesity, Proprotein Convertase 1
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 0012-1797
العلاقة: Diabetes; http://hdl.handle.net/10044/1/28719Test; https://dx.doi.org/10.2337/db11-0305Test; G0801056B; G0801056/1
DOI: 10.2337/db11-0305
الإتاحة: https://doi.org/10.2337/db11-0305Test
http://hdl.handle.net/10044/1/28719Test
حقوق: © 2012 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0Test/ for details.
رقم الانضمام: edsbas.C36CA299
قاعدة البيانات: BASE
الوصف
تدمد:00121797
DOI:10.2337/db11-0305