Insights into the molecular mechanism for type 2 diabetes susceptibility at the KCNQ1 locus from temporal changes in imprinting status in human islets. [electronic resource]
- Diabetes Mar 2013
- 987-92 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1939-327X
10.2337/db12-0819 doi
Adult Alleles Chromosomes, Human, Pair 11--genetics Cohort Studies Cyclin-Dependent Kinase Inhibitor p57--genetics DNA Methylation Diabetes Mellitus, Type 2--genetics Fetal Development Gene Expression Regulation, Developmental Genetic Association Studies Genetic Loci Genetic Predisposition to Disease Humans Introns Islets of Langerhans--growth & development KCNQ1 Potassium Channel--genetics Pancreas--embryology Polymorphism, Single Nucleotide Potassium Channels, Voltage-Gated--genetics United Kingdom