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Q48167097-7A133682-976F-425D-B54B-B9606F96E138
Q48167097-7A133682-976F-425D-B54B-B9606F96E138
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http://www.wikidata.org/entity/statement/Q48167097-7A133682-976F-425D-B54B-B9606F96E138
Homozygous p.V116* mutation in C12orf65 results in Leigh syndrome.
P2860
Q48167097-7A133682-976F-425D-B54B-B9606F96E138
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48167097-7A133682-976F-425D-B54B-B9606F96E138
rank
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Statement
wasDerivedFrom
dc37a2ab76d64fd4077439d078d871e4c12d62ac
P2860
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy.