Homozygous Nonsense Mutation in the FOXE3 Gene as a Cause of Congenital Primary Aphakia in Humans-Reference-Cited by-同舟云学术

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Homozygous Nonsense Mutation in the FOXE3 Gene as a Cause of Congenital Primary Aphakia in Humans

Published:2006-08 Issue:2 Volume:79 Page:358-364
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Valleix Sophie,Niel Florence,Nedelec Brigitte,Algros Marie-Paule,Schwartz Claire,Delbosc Bernard,Delpech Marc,Kantelip Bernadette

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference29 articles.

1. The lens organizes the anterior segment: specification of neural crest cell differentiation in the avian eye;Beebe;Dev Biol,2000

2. Anterior segment development relevant to glaucoma;Gould;Int J Dev Biol,2004

3. Cataract mutations and lens development;Graw;Prog Retin Eye Res,1999

4. Primary congenital aphakia;Manschot;Arch Ophthalmol,1963

5. Embryology of the eye and its adnexae;Barishak;Dev Ophthalmol,1992

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