𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Identification of three missense mutations in the peroxisome proliferator-activated receptor α gene in Japanese subjects with maturity-onset diabetes of the young

✍ Scribed by M. Hara; X. Wang; V. P. Paz; N. Iwasaki; M. Honda; Y. Iwamoto; G. I. Bell


Publisher
Nature Publishing Group
Year
2001
Tongue
English
Weight
60 KB
Volume
46
Category
Article
ISSN
1435-232X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Three novel missense mutations in the gl
✍ Barbara Guazzini; Davide Gaffi; Davide Mainieri; Giuseppe Multari; Renzo Cordera 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 30 KB 👁 1 views

The maturity-onset diabetes of the young (MODY), an autosomal dominant form of non-insulin dependent diabetes mellitus (NIDDM), is caused by mutations in the glucokinase (GK, MODY 2) and in the hepatocyte nuclear factor 1 (MODY 3) and 4 (MODY1) genes. We have screened the glucokinase gene by the pol

Identification of eight novel glucokinas
✍ Vilma Mantovani; Silvana Salardi; Vincenzo Cerreta; Daniela Bastia; Marinella Ce 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 35 KB 👁 2 views

## Maturity -onset diabetes of the young (MODY) is a clinically heterogeneous group of disorders characterized by early onset non-insulin-dependent diabetes mellitus, autosomal dominant inheritance, and primary defect in the function of the beta cells of the pancreas. Mutations in the glucokinase

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