✦ LIBER ✦

HeterozygousABCC8mutations are a cause of MODY

✍ Scribed by P. Bowman; S. E. Flanagan; E. L. Edghill; A. Damhuis; M. H. Shepherd; R. Paisey; A. T. Hattersley; S. Ellard

Book ID: 105820394
Publisher: Springer
Year: 2011
Tongue: English
Weight: 150 KB
Volume: 55
Category: Article
ISSN: 0012-186X
DOI: 10.1007/s00125-011-2319-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutations in theSLC30A8gene are not a ma

Mutations in theSLC30A8gene are not a major cause of MODY or other forms of early-onset, autosomal dominant type 2 diabetes

✍ M. Borowiec; R. Thompson; C. Powers; R. Xu; T. Dickey; A. Doria 📂 Article 📅 2007 🏛 Springer 🌐 English ⚖ 80 KB

miRNA mutations are not a common cause o

miRNA mutations are not a common cause of deafness

✍ Michael S. Hildebrand; P. Dane Witmer; Shunbin Xu; Stephen S. Newton; Kimia Kahr 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 184 KB 👁 2 views

Rare β-thalassemia mutations are cause o

Rare β-thalassemia mutations are cause of concern

✍ Anju Gupta; Sarita Agarwal 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 84 KB 👁 1 views

Deep intronic mutations are rarely a cau

Deep intronic mutations are rarely a cause of hemophilia B

✍ Jinong Feng; Qiang Liu; Joni Drost; Steve S. Sommer 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 89 KB 👁 2 views

NTNG1 mutations are a rare cause of Rett

NTNG1 mutations are a rare cause of Rett syndrome

✍ Hayley L. Archer; Julie C. Evans; David S. Millar; Peter W. Thompson; Alison M. 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 86 KB 👁 2 views

Mutations in PEX10 are a cause of autoso

Mutations in PEX10 are a cause of autosomal recessive ataxia

✍ Luc Régal; Merel S. Ebberink; Nathalie Goemans; Ronald J. A. Wanders; Linda De M 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 173 KB 👁 1 views