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Q51728986-7E920F82-6D56-4291-B78D-B146061B481C
Q51728986-7E920F82-6D56-4291-B78D-B146061B481C
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http://www.wikidata.org/entity/statement/Q51728986-7E920F82-6D56-4291-B78D-B146061B481C
m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.
P2860
Q51728986-7E920F82-6D56-4291-B78D-B146061B481C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51728986-7E920F82-6D56-4291-B78D-B146061B481C
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Statement
wasDerivedFrom
d11dc827aa5acf8521327ac004cf23e43e0f5f7f
P2860
Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.