𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutations inKCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6

✍ Scribed by S. E. Flanagan; E. L. Edghill; A. L. Gloyn; S. Ellard; A. T. Hattersley


Publisher
Springer
Year
2006
Tongue
English
Weight
239 KB
Volume
49
Category
Article
ISSN
0012-186X

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Mutations in the first MyTH4 domain of M
✍ A. Eliot Shearer; Michael S. Hildebrand; Jennifer A. Webster; Kimia Kahrizi; Nic πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 679 KB

## Abstract ## Objectives. To use clinical and genetic analyses to determine the mutation causing autosomal recessive nonsyndromic hearing loss (ARNSHL) segregating in two consanguineous Iranian families. ## Study Design. Family study. ## Methods. Members of each family received otologic and a