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Novel Presentations of Congenital Hyperinsulinism due to Mutations in the MODY genes: HNF1A and HNF4A

✍ Scribed by Stanescu, D. E.; Hughes, N.; Kaplan, B.; Stanley, C. A.; De Leon, D. D.

Book ID: 115481540
Publisher: Endocrine Society
Year: 2012
Tongue: English
Weight: 144 KB
Volume: 97
Category: Article
ISSN: 0021-972X
DOI: 10.1210/jc.2012-1356

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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