Different Functional Outcome of RetGC1 and RPE65 Gene Mutations in Leber Congenital Amaurosis-Reference-Cited by-同舟云学术

Different Functional Outcome of RetGC1 and RPE65 Gene Mutations in Leber Congenital Amaurosis

Published:1999-04 Issue:4 Volume:64 Page:1225-1228
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Perrault Isabelle,Rozet Jean-Michel,Ghazi Imad,Leowski Corinne,Bonnemaison Michèle,Gerber Sylvie,Ducroq Dominique,Cabot Annick,Souied Eric,Dufier Jean-Louis,Munnich Arnold,Kaplan Josseline

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference14 articles.

1. A gene for Leber's congenital amaurosis maps to chromosome 17p;Camuzat;Hum Mol Genet,1995

2. Evidence of genetic heterogeneity of Leber's congenital amaurosis (LCA) and mapping of LCA1 to chromosome 17p13;Camuzat;Hum Genet,1996

3. Classification of congenital and early-onset retinitis pigmentosa;Foxman;Arch Ophthalmol,1985

4. L'importance diagnostique de l'électrorétinogramme dans les dégénérescences tapéto-rétiniennes avec rétrécissement du champ visuel et héméralopie;Franceschetti;Conf Neuro,1954

5. Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy;Gu;Nat Genet,1997

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