๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Novel mutations in GCK and HNF1A genes in Italian families with MODY phenotype

โœ Scribed by Alessia Cappelli; Stefano Tumini; Agostino Consoli; Silvia Carinci; Concettina Piersanti; Giuseppina Ruggiero; Graziano Simonella; Filippo Soletti; Paolo Staffolani; Luigi Pianese

Book ID
116406436
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
166 KB
Volume
83
Category
Article
ISSN
0168-8227

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

GCK and HNF1A mutations in Canadian fami
GCK and HNF1A mutations in Canadian families with maturity onset diabetes of the young (MODY)
โœ Henian Cao; Sanam Shorey; John Robinson; Daniel L. Metzger; Laura Stewart; Eliza ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 28 KB ๐Ÿ‘ 2 views

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

Identification of novel GCK and HNF1A/TC
Identification of novel GCK and HNF1A/TCF1 mutations and polymorphisms in German families with maturity-onset diabetes of the young (MODY)
โœ Dalia Toaima; Andrea Nรคke; Jutta Wendenburg; Kirsten Praedicow; Julia Rohayem; K ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 74 KB ๐Ÿ‘ 2 views

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