Maturity-onset diabetes of the young caused by a balanced translocation where the 20q12 break point results in disruption upstream of the coding region of hepatocyte nuclear factor-4alpha (HNF4A) gene.
Monogenic human disorders have been used as paradigms for complex genetic disease and as tools for establishing important insights into mechanisms of gene regulation and transcriptional control. Maturity-onset diabetes of the young (MODY) is a monogenic dominantly inherited form of diabetes that is...
المؤلفون الرئيسيون: | Gloyn, A, Ellard, S, Shepherd, M, Howell, RT, Parry, E, Jefferson, A, Levy, E, Hattersley, A |
---|---|
التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2002
|
مواد مشابهة
-
The role of the HNF4alpha enhancer in type 2 diabetes.
حسب: Mitchell, S, وآخرون
منشور في: (2002) -
The role of the HNF4α enhancer in type 2 diabetes variants of the HNF4α enhancer are not a common cause of susceptibility to type 2 diabetes
حسب: Mitchell, S, وآخرون
منشور في: (2002) -
Species-specific differences in the expression of the HNF1A, HNF1B and HNF4A genes.
حسب: Harries, L, وآخرون
منشور في: (2009) -
Species-specific differences in the expression of the HNF1A, HNF1B and HNF4A genes.
حسب: Lorna W Harries, وآخرون
منشور في: (2009-11-01) -
High-sensitivity CRP discriminates HNF1A-MODY from other subtypes of diabetes.
حسب: McDonald, T, وآخرون
منشور في: (2011)