High Prevalence of PRPH2 in Autosomal Dominant Retinitis Pigmentosa in France and Characterization of Biochemical and Clinical Features-Reference-Cited by-同舟云学术

High Prevalence of PRPH2 in Autosomal Dominant Retinitis Pigmentosa in France and Characterization of Biochemical and Clinical Features

Published:2015-02 Issue:2 Volume:159 Page:302-314
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Manes Gaël,Guillaumie Tremeur,Vos Werner L.,Devos Aurore,Audo Isabelle,Zeitz Christina,Marquette Virginie,Zanlonghi Xavier^ORCID,Defoort-Dhellemmes Sabine,Puech Bernard,Said Saddek Mohand,Sahel José Alain,Odent Sylvie,Dollfus Hélène,Kaplan Josseline,Dufier Jean-Louis,Le Meur Guylène,Weber Michel,Faivre Laurence,Cohen Francine Behar,Béroud Christophe,Picot Marie-Christine,Verdier Coralie,Sénéchal Audrey,Baudoin Corinne,Bocquet Béatrice,Findlay John B.,Meunier Isabelle,Dhaenens Claire-Marie,Hamel Christian P.

Funder

Union Nationale des Aveugles et Déficients Visuels

foundation Voir et Entendre

foundation Fighting Blindness

Fondation Dalloz

Publisher

Elsevier BV

Subject

Ophthalmology

Reference55 articles.

1. Localization of peripherin/rds in the disk membranes of cone and rod photoreceptors: relationship to disk membrane morphogenesis and retinal degeneration;Arikawa;J Cell Biol,1992

2. Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse;Connell;Proc Natl Acad Sci U S A,1991