A novel OPA1 mutation causing variable age of onset autosomal dominant optic atrophy plus in an Australian family
Crossref DOI link: https://doi.org/10.1007/s00415-015-7849-6
Published Online: 2015-07-21
Published Print: 2015-10
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Ahmad, K. E.
Davis, R. L.
Sue, C. M.
Funding for this research was provided by:
NHMRC (1074763)
NHMRC (1037797)
National Health and Medical Research Council (1008433)
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