Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Clinical Neurology,Molecular Biology,General Neuroscience
Reference33 articles.
1. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nat. Genet.,2000
2. OPA1 R445H mutation in optic atrophy associated with sensorineural deafness;Amati-Bonneau;Ann. Neurol.,2005
3. OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes;Amati-Bonneau;Brain,2008
4. Cochlear implantation in deafness-dystonia-optic neuronopathy (DDON) syndrome;Brookes;J. Pediatr. Orhinolaryngol.,2008
5. Mitochondrial dysfunction as a cause of optic neuropathies;Carelli;Prog. Retin. Eye Res.,2004
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