OPA1 expression in the human retina and optic nerve
Author:
Publisher
Elsevier BV
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Reference30 articles.
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2. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nat. Genet.,2000
3. Fourteen novel OPA1 mutations in autosomal dominant optic atrophy including two de novo mutations in sporadic optic atrophy;Baris;Hum. Mutat.,2003
4. No evidence of genetic heterogeneity in dominant optic atrophy;Bonneau;J. Med. Genet.,1995
5. Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy;Delettre;Nat. Genet.,2000
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