Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness

Author:

Vincent Ajoy,Audo Isabelle,Tavares Erika,Maynes Jason T.,Tumber Anupreet,Wright Thomas,Li Shuning,Michiels Christelle,Condroyer Christel,MacDonald Heather,Verdet Robert,Sahel José-Alain,Hamel Christian P.,Zeitz Christina,Héon Elise,Banin Eyal,Bocquet Beatrice,De Baere Elfride,Casteels Ingele,Defoort-Dhellemmes Sabine,Drumare Isabelle,Friedburg Christoph,Gottlob Irene,Jacobson Samuel G.,Kellner Ulrich,Koenekoop Robert,Kohl Susanne,Leroy Bart P.,Lorenz Birgit,McLean Rebecca,Meire Francoise,Meunier Isabelle,Munier Francis,de Ravel Thomy,Reiff Charlotte M.,Mohand-Saïd Saddek,Sharon Dror,Schorderet Daniel,Schwartz Sharon,Zanlonghi Xavier

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference72 articles.

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4. A proximal retinal component in the primate photopic ERG a-wave;Bush;Invest. Ophthalmol. Vis. Sci.,1994

5. Inner retinal contributions to the primate photopic fast flicker electroretinogram;Bush;J. Opt. Soc. Am. A Opt. Image Sci. Vis.,1996

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