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OPA1
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy
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
OPTN
Identification and characterization of a family of Rab11-interacting proteins
Expression of optineurin, a glaucoma-linked gene, is influenced by elevated intraocular pressure
Optineurin gene expression level in human trabecular meshwork does not change in response to pressure elevation
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