Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy-Reference-Cited by-同舟云学术

Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy

Published:2010-02 Issue:2 Volume:86 Page:248-253
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Poulter James A.,Ali Manir,Gilmour David F.,Rice Aine,Kondo Hiroyuki,Hayashi Kenshi,Mackey David A.,Kearns Lisa S.,Ruddle Jonathan B.,Craig Jamie E.,Pierce Eric A.,Downey Louise M.,Mohamed Moin D.,Markham Alexander F.,Inglehearn Chris F.,Toomes Carmel

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference33 articles.

1. Familial exudative vitreoretinopathy;Criswick;Am. J. Ophthalmol.,1969

2. Familial exudative vitreoretinopathy;Benson;Trans. Am. Ophthalmol. Soc.,1995

3. A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy;Chen;Nat. Genet.,1993

4. Mutant Frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy;Robitaille;Nat. Genet.,2002

5. Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q;Toomes;Am. J. Hum. Genet.,2004

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