𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry

✍ Scribed by Jørn V Sagen; Lise Bjørkhaug; Janne Molnes; Helge Ræder; Louise Grevle; Oddmund Søvik; Anders Molven; Pål R Njølstad


Book ID
110905601
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
221 KB
Volume
9
Category
Article
ISSN
1399-543X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


GCK and HNF1A mutations in Canadian fami
✍ Henian Cao; Sanam Shorey; John Robinson; Daniel L. Metzger; Laura Stewart; Eliza 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 28 KB 👁 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 21 novel glucokinase (
✍ K.L. Thomson; A.L. Gloyn; K. Colclough; M. Batten; L.I.S. Allen; F. Beards; A.T. 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 32 KB 👁 2 views

## Maturity -onset diabetes of the young (MODY) resulting from mutations in the glucokinase (GCK) gene accounts for approximately 20% of MODY in the UK. W e have performed fluorescent single stranded conformation polymorphism (F-SSCP) analysis or direct sequencing of the GCK gene in 212 patients re