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Q38626524-700FC78E-DD76-4E28-A5D5-29B482C15A90
Q38626524-700FC78E-DD76-4E28-A5D5-29B482C15A90
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http://www.wikidata.org/entity/statement/Q38626524-700FC78E-DD76-4E28-A5D5-29B482C15A90
Autopsy case of the C12orf65 mutation in a patient with signs of mitochondrial dysfunction.
P2860
Q38626524-700FC78E-DD76-4E28-A5D5-29B482C15A90
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38626524-700FC78E-DD76-4E28-A5D5-29B482C15A90
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wasDerivedFrom
d5ab2c0c46481e15ea8f14aad0f0a48fd6a32c00
P2860
A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55).