Prime suspect: the TCF7L2 gene and type 2 diabetes risk
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference25 articles.
1. Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes
2. The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
3. Large-Scale Association Studies of Variants in Genes Encoding the Pancreatic β-Cell KATP Channel Subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) Confirm That the KCNJ11 E23K Variant Is Associated With Type 2 Diabetes
4. Dominant negative mutations in human PPARγ associated with severe insulin resistance, diabetes mellitus and hypertension
5. Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes
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