✦ LIBER ✦

Variable phenotypic spectrum of diabetes mellitus in a family carrying a novel KCNJ11 gene mutation

✍ Scribed by E. D’Amato; P. Tammaro; T. J. Craig; A. Tosi; R. Giorgetti; R. Lorini; F. M. Ashcroft

Book ID: 110925424
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 189 KB
Volume: 25
Category: Article
ISSN: 0742-3071
DOI: 10.1111/j.1464-5491.2008.02443.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Phenotype variability and neonatal diabe

Phenotype variability and neonatal diabetes in a large family with heterozygous mutation of the glucokinase gene

✍ Maciej Borowiec; Malgorzata Mysliwiec; Wojciech Fendler; Karolina Antosik; Agnie 📂 Article 📅 2011 🏛 Springer 🌐 English ⚖ 344 KB

A novel mutation of the familial Mediter

A novel mutation of the familial Mediterranean fever gene in a Greek family related to a non-classical, variably expressed FMF phenotype

✍ Dimitrios Zonios; Clio P. Mavragani; Stavros Giaglis; Konstatinos Ritis 📂 Article 📅 2007 🏛 Springer 🌐 English ⚖ 201 KB

A novel frameshift mutation ofFOXC2 gene

A novel frameshift mutation ofFOXC2 gene in a family with hereditary lymphedema-distichiasis syndrome associated with renal disease and diabetes mellitus

✍ Yildirim-Toruner, Cagri ;Subramanian, Kavitha ;El Manjra, Lamya ;Chen, Emily ;Go 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 208 KB 👁 2 views

Type 2 (non-insulin-dependent) diabetes

Type 2 (non-insulin-dependent) diabetes mellitus associated with a mutation of the glucokinase gene in a Japanese family

✍ F. Shimada; H. Makino; N. Hashimoto; M. Taira; S. Seino; G. I. Bell; A. Kanatsuk 📂 Article 📅 1993 🏛 Springer 🌐 English ⚖ 803 KB

Mutations were screened for in the glucokinase gene of 25 Japanese patients with Type 2 (non-insulin-dependent) diabetes mellitus. Each exon was scanned by electrophoresis of enzymatically amplified DNA segments under non-denaturing conditions and variants were sequenced. A variant pattern was detec

Novel mutation in theNHLRC1gene in a Mal

Novel mutation in theNHLRC1gene in a Malian family with a severe phenotype of Lafora disease

✍ M. Traoré; G. Landouré; W. Motley; M. Sangaré; K. Meilleur; S. Coulibaly; S. Tra 📂 Article 📅 2009 🏛 Springer 🌐 English ⚖ 148 KB

Association between KCNJ11 gene polymorp

Association between KCNJ11 gene polymorphisms and risk of type 2 diabetes mellitus in East Asian populations: a meta-analysis in 42,573 individuals

✍ Lijuan Yang; Xianghai Zhou; Yingying Luo; Xiuqin Sun; Yong Tang; Wulan Guo; Xuey 📂 Article 📅 2011 🏛 Springer 🌐 English ⚖ 407 KB