The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness-Reference-Cited by-同舟云学术

The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness

Published:1995-08 Issue:16 Volume:35 Page:2383-2393
ISSN:0042-6989
Container-title:Vision Research
language:en
Short-container-title:Vision Research

Author:

Tremblay François,Laroche Robert G.,De Becker Inge

Publisher

Elsevier BV

Subject

Sensory Systems,Ophthalmology

Reference39 articles.

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2. An electrophysiological and psychophysical study of two forms of congenital night blindness;Auerbach;Investigative Ophthalmology and Visual Science,1969

3. Blindness from quinine toxicity;Bacon;British Journal of Ophthalmology,1988

4. Genetic and clinical correlations of Xp21 Muscular Dystrophy;Bushby;Journal of Inherited Metabolic Disorders,1992

5. Congenital stationary night blindness;Carr,1991

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1. Diagnosis of an X-linked type 2 congenital stationary night blindness using electroretinography and CACNA1F sequencing;Archivos de la Sociedad Española de Oftalmología (English Edition);2020-12

2. Diagnóstico de un caso de ceguera nocturna estacionaria congénita tipo 2 ligada al cromosoma X mediante electrorretinografía y secuenciación del gen CACNA1F;Archivos de la Sociedad Española de Oftalmología;2020-12

3. Transgenic Expression of Cacna1f Rescues Vision and Retinal Morphology in a Mouse Model of Congenital Stationary Night Blindness 2A (CSNB2A);Translational Vision Science & Technology;2020-10-14

4. An Ashkenazi Jewish founder mutation in CACNA1F causes retinal phenotype in both hemizygous males and heterozygous female carriers;Ophthalmic Genetics;2019-09-03

5. Clinical Characteristics, Mutation Spectrum, and Prevalence of Åland Eye Disease/Incomplete Congenital Stationary Night Blindness in Denmark;Investigative Opthalmology & Visual Science;2016-12-21