𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The Type and the Position of HNF1A Mutation Modulate Age at Diagnosis of Diabetes in Patients with Maturity-Onset Diabetes of the Young (MODY)-3

✍ Scribed by Bellanne-Chantelot, C.; Carette, C.; Riveline, J.-P.; Valero, R.; Gautier, J.-F.; Larger, E.; Reznik, Y.; Ducluzeau, P.-H.; Sola, A.; Hartemann-Heurtier, A.; Lecomte, P.; Chaillous, L.; Laloi-Michelin, M.; Wilhem, J.-M.; Cuny, P.; Duron, F.; Guerci, B.; Jeandidier, N.; Mosnier-Pudar, H.; Assayag, M.; Dubois-Laforgue, D.; Velho, G.; Timsit, J.


Book ID
121341436
Publisher
American Diabetes Association
Year
2007
Tongue
English
Weight
119 KB
Volume
57
Category
Article
ISSN
0012-1797

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


GCK and HNF1A mutations in Canadian fami
✍ Henian Cao; Sanam Shorey; John Robinson; Daniel L. Metzger; Laura Stewart; Eliza πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 28 KB πŸ‘ 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
✍ Dalia Toaima; Andrea NΓ€ke; Jutta Wendenburg; Kirsten Praedicow; Julia Rohayem; K πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 74 KB πŸ‘ 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