Unexplained visual loss
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference18 articles.
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2. Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1);Brown;Arch Ophthalmol,1997
3. Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy;Delettre;Nat Genet,2000
4. Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis;Eiberg;Hum Mol Genet,1994
5. Autosomal dominant optic atrophy. A spectrum of disability;Hoyt;Ophthalmology,1980
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