Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans-Reference-Cited by-同舟云学术

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Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans

Published:2013-03-27 Issue:12 Volume:21 Page:1356-1360
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Berry Vanita,Gregory-Evans Cheryl,Emmett Warren,Waseem Naushin,Raby Jacob,Prescott DeQuincy,Moore Anthony T,Bhattacharya Shomi S

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg201352.pdf

Reference20 articles.

1. Reddy MA, Francis PA, Berry V, Bhattacharya SS, Moore AT : Molecular genetic basis of inherited cataract and associated phenotypes. Surv Ophthalmol 2004; 49: 300–315.

2. Krumpaszky HG, Klauss V : Epidemiology of blindness and eye disease. Ophthalmologica 1996; 210: 1–84.

3. Francis PJ, Berry V, Bhattacharya SS, Moore AT : The genetics of childhood cataract. J Med Genet 2000a; 37: 481–488.

4. Shiels A, Bennett TM, Hejtmancik JF : Cat-Map: putting cataract on the map. Mol Vis 2010; 16: 2007–2015.

5. Schmidt-Kastner R, Kreczmanski P, Preising M et al: Expression of the diabetes risk gene wolframin (WFS1) in the human retina. Exp Eye Res 2009; 89: 568–574.

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