No evidence of genetic heterogeneity in dominant optic atrophy.

Autosomal dominant optic atrophy (OPA, MIM 165500) is an eye disease causing a variable reduction of visual acuity with an insidious onset in the first six years of life. It is associated with a central scotoma and an acquired blue-yellow dyschromatopsia. A gene for dominant optic atrophy (OPA1) has...

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Detalles Bibliográficos
Main Authors: Bonneau, D, Souied, E, Gerber, S, Rozet, J M, D'Haens, E, Journel, H, Plessis, G, Weissenbach, J, Munnich, A, Kaplan, J
Formato: Artigo
Idioma:Inglês
Publicado: 1995
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051775/
https://ncbi.nlm.nih.gov/pubmed/8825922
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