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Q42236974-3FB4A9E1-21FA-4C78-B24D-380CE1971D65
Q42236974-3FB4A9E1-21FA-4C78-B24D-380CE1971D65
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42236974-3FB4A9E1-21FA-4C78-B24D-380CE1971D65
Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations
P2860
Q42236974-3FB4A9E1-21FA-4C78-B24D-380CE1971D65
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42236974-3FB4A9E1-21FA-4C78-B24D-380CE1971D65
rank
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type
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wasDerivedFrom
39c310ff1d9debc0436a6bdb886e8ddc82fb7d6b
P2860
'Behr syndrome' with OPA1 compound heterozygote mutations.