Progressive juvenile-onset punctate cataracts caused by mutation of the D-crystallin gene-Reference-Cited by-同舟云学术

Progressive juvenile-onset punctate cataracts caused by mutation of the D-crystallin gene

Published:1999-02-02 Issue:3 Volume:96 Page:1008-1012
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Stephan D. A.,Gillanders E.,Vanderveen D.,Freas-Lutz D.,Wistow G.,Baxevanis A. D.,Robbins C. M.,Van Auken A.,Quesenberry M. I.,Bailey-Wilson J.,Juo S.-H. H.,Trent J. M.,Smith L.,Brownstein M. J.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference17 articles.

1. INVITED EDITORIAL The Genetics of Cataract: Our Vision Becomes Clearer

2. Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA

3. Autosomal Dominant Cerulean Cataract Is Associated with a Chain Termination Mutation in the Human -Crystallin Gene CRYBB2

4. Activation of the ΓE-crystallin pseudogene in the human hereditary Coppock-like cataract

5. A Missense Mutation in the Human Connexin50 Gene (GJA8) Underlies Autosomal Dominant “Zonular Pulverulent” Cataract, on Chromosome 1q

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