Replication of the association between variants in the WFS1 gene and risk of type 2 diabetes in European populations

AIMS/HYPOTHESIS: Mutations at the Wolframin encoding gene, WFS1, cause Wolfram syndrome, a rare neurological condition. Associations between single nucleotide polymorphisms (SNPs) at WFS1 and type 2 diabetes have recently been reported. In the present study, we sought to replicate those associations...

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書誌詳細
主要な著者: Franks, P.W., Rolandsson, O., Debenham, S.L., Fawcett, K.A., Payne, F., Dina, C., Froguel, P., Mohlke, K.L., Willer, C., Olsson, T., Wareham, N.J., Hallmans, G., Barroso, I, Sandhu, M.S.
フォーマット: Artigo
言語:Inglês
出版事項: 2007
主題:
Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2670195/
https://ncbi.nlm.nih.gov/pubmed/18040659
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00125-007-0887-6
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