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Q36023873-A07C7BBC-C197-4648-A17A-B0A23D7489E7
Q36023873-A07C7BBC-C197-4648-A17A-B0A23D7489E7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36023873-A07C7BBC-C197-4648-A17A-B0A23D7489E7
Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients.
P2860
Q36023873-A07C7BBC-C197-4648-A17A-B0A23D7489E7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36023873-A07C7BBC-C197-4648-A17A-B0A23D7489E7
rank
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type
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Statement
wasDerivedFrom
6603db8acd177a83f9bf245ae69f06505d34604f
P2860
Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.