Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness-Reference-Cited by-同舟云学术

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

Published:2012-02 Issue:2 Volume:90 Page:321-330
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Audo Isabelle,Bujakowska Kinga,Orhan Elise,Poloschek Charlotte M.,Defoort-Dhellemmes Sabine,Drumare Isabelle,Kohl Susanne,Luu Tien D.,Lecompte Odile,Zrenner Eberhart,Lancelot Marie-Elise,Antonio Aline,Germain Aurore,Michiels Christelle,Audier Claire,Letexier Mélanie,Saraiva Jean-Paul,Leroy Bart P.,Munier Francis L.,Mohand-Saïd Saddek,Lorenz Birgit,Friedburg Christoph,Preising Markus,Kellner Ulrich,Renner Agnes B.,Moskova-Doumanova Veselina,Berger Wolfgang,Wissinger Bernd,Hamel Christian P.,Schorderet Daniel F.,De Baere Elfride,Sharon Dror,Banin Eyal,Jacobson Samuel G.,Bonneau Dominique,Zanlonghi Xavier,Le Meur Guylene,Casteels Ingele,Koenekoop Robert,Long Vernon W.,Meire Francoise,Prescott Katrina,de Ravel Thomy,Simmons Ian,Nguyen Hoan,Dollfus Hélène,Poch Olivier,Léveillard Thierry,Nguyen-Ba-Charvet Kim,Sahel José-Alain,Bhattacharya Shomi S.,Zeitz Christina

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference47 articles.

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4. The negative ERG: Clinical phenotypes and disease mechanisms of inner retinal dysfunction;Audo;Surv. Ophthalmol.,2008

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