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Q30368414-CDEC8F91-36D8-403B-BF4C-541B55045B7C
Q30368414-CDEC8F91-36D8-403B-BF4C-541B55045B7C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30368414-CDEC8F91-36D8-403B-BF4C-541B55045B7C
A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family
P2860
Q30368414-CDEC8F91-36D8-403B-BF4C-541B55045B7C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30368414-CDEC8F91-36D8-403B-BF4C-541B55045B7C
rank
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type
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Statement
wasDerivedFrom
79b876d0bac50aea9685a8ebf3ab0fa70e5052c5
P2860
Mutation of OPA1 gene causes deafness by affecting function of auditory nerve terminals.