Clinical assessment of HNF1A and GCK variants and identification of a novel mutation causing MODY2
โ Scribed by Ashley H. Shoemaker; Jozef Zienkiewicz; Daniel J. Moore
- Book ID
- 116407432
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 517 KB
- Volume
- 96
- Category
- Article
- ISSN
- 0168-8227
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๐ SIMILAR VOLUMES
Maturity-onset diabetes of the young is a genetically heterogenous autosomal dominant form of diabetes mellitus, characterized by an early age at onset and a primary defect in beta-cell function. Forty families with a clinical presentation suggestive of MODY were screened for the most common MODY su
Maturity onset diabetes of the young (MODY) is a genetically heterogeneous form of type 2 diabetes that is characterized by autosomal dominant inheritance, onset in early adulthood and a primary defect in insulin secretion. Mutations in at least six genes have been shown to underlie MODY, including