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Q48167097-16A27A9D-3A0F-4D73-A419-13C1EF1FB4AF
Q48167097-16A27A9D-3A0F-4D73-A419-13C1EF1FB4AF
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http://www.wikidata.org/entity/statement/Q48167097-16A27A9D-3A0F-4D73-A419-13C1EF1FB4AF
Homozygous p.V116* mutation in C12orf65 results in Leigh syndrome.
P2860
Q48167097-16A27A9D-3A0F-4D73-A419-13C1EF1FB4AF
BestRank
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http://www.wikidata.org/entity/statement/Q48167097-16A27A9D-3A0F-4D73-A419-13C1EF1FB4AF
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wasDerivedFrom
dc37a2ab76d64fd4077439d078d871e4c12d62ac
P2860
A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55).