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searching for OPA3 3 found (9 total)

alternate case: oPA3

Behr syndrome (782 words) [view diff] exact match in snippet view article find links to article

described. Some reported cases have been found to carry mutations in the OPA1, OPA3 or C12ORF65 genes which are known causes of pure optic atrophy or optic atrophy

Wolfram syndrome (5,032 words) [view diff] exact match in snippet view article find links to article

tested negative for mutation in the common optic neuropathy genes OPA1, OPA3 and LHON were selected for further genetic testing for WS. The primary genetic

Kjer's optic neuropathy (2,012 words) [view diff] exact match in snippet view article find links to article

chromosomal genes are described as causing optic atrophy: OPA2 (x-linked), OPA3 (dominant), OPA4 (dominant), OPA5 (dominant) and OPA6 (recessive) (see OMIM