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Q51728986-1851F39C-0408-46D1-981E-B976CC1AD76C
Q51728986-1851F39C-0408-46D1-981E-B976CC1AD76C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51728986-1851F39C-0408-46D1-981E-B976CC1AD76C
m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.
P407
Q51728986-1851F39C-0408-46D1-981E-B976CC1AD76C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51728986-1851F39C-0408-46D1-981E-B976CC1AD76C
rank
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type
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P407
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