Dominant Optic Atrophy: Novel OPA1 Mutations and Revised Prevalence Estimates
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference5 articles.
1. The prevalence and natural history of dominant optic atrophy due to OPA1 mutations;Yu-Wai-Man;Ophthalmology,2010
2. Mitochondrial optic neuropathies: disease mechanisms and therapeutic strategies;Yu-Wai-Man;Prog Retin Eye Res,2011
3. Dominant optic atrophy;Lenaers;Orphanet J Rare Dis,2012
4. Multi-system neurological disease is common in patients with OPA1 mutations;Yu-Wai-Man;Brain,2010
5. A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect;Thiselton;Hum Genet,2001
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