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

AIMS/HYPOTHESIS: More than 90% of Chinese familial early-onset type 2 diabetes mellitus is genetically unexplained. To investigate the molecular aetiology, we identified and characterised whether mutations in the KCNJ11 gene are responsible for these families. METHODS: KCNJ11 mutations were screened...

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Pubblicato in:Diabetologia
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2013
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5333983/
https://ncbi.nlm.nih.gov/pubmed/24018988
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00125-013-3031-9
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