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

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اقرأ أكثر حفظ في قائمتي

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
المصدر:
390 ; 383
الموضوع:
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 التسجيلة:
article in journal/newspaper
اللغة:
English

معلومة اضافية
- Contributors:
  Medical Research Council (MRC)
- بيانات النشر:
  American Diabetes Association
- الموضوع:
  2011
- Collection:
  Imperial College London: Spiral
- ISSN:
  0012-1797
- Relation:
  Diabetes; http://hdl.handle.net/10044/1/28719; https://dx.doi.org/10.2337/db11-0305; G0801056B; G0801056/1
- الرقم المعرف:
  10.2337/db11-0305
- Rights:
  © 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/3.0/ for details.
- الرقم المعرف:
  edsbas.C36CA299

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