Mutations in KCNJ11 are associated with the development of autosomal dominant, early-onset type 2 diabetes-Reference-Cited by-同舟云学术

Mutations in KCNJ11 are associated with the development of autosomal dominant, early-onset type 2 diabetes

Published:2013-09-10 Issue:12 Volume:56 Page:2609-2618
ISSN:0012-186X
Container-title:Diabetologia
language:en
Short-container-title:Diabetologia

Author:

Liu Limei,Nagashima Kazuaki,Yasuda Takao,Liu Yanjun,Hu Hai-rong,He Guang,Feng Bo,Zhao Mingming,Zhuang Langen,Zheng Taishan,Friedman Theodore C.,Xiang Kunsan

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00125-013-3031-9.pdf

Reference44 articles.

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2. American Diabetes Association (2013) Diagnosis and classification of diabetes mellitus. Diabetes Care 36(Suppl 1):S67–S74

3. Fajans SS, Bell GI (2011) MODY: history, genetics, pathophysiology, and clinical decision making. Diabetes Care 34:1878–1884

4. Doria A, Yang Y, Malecki M et al (1999) Phenotypic characteristics of early-onset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes. Diabetes Care 22:253–261

5. Gloyn AL, Pearson ER, Antcliff JF et al (2004) Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes. N Engl J Med 350:1838–1849

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