Genetic Heterogeneity of Dominant Optic Atrophy, Kjer Type
Open Access
- 1 June 1999
- journal article
- ophthalmic molecular-genetics
- Published by American Medical Association (AMA) in Archives of Ophthalmology (1950)
- Vol. 117 (6), 805-810
- https://doi.org/10.1001/archopht.117.6.805
Abstract
AUTOSOMAL dominant optic atrophy (Mendelian Inheritance in Man 165500 1) is a hereditary disorder characterized by bilateral insidious onset of vision loss, dyschromatopsia, central visual field defects, and optic nerve pallor.2-5 The gene is highly penetrant and has variable expressivity.Keywords
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