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Q34064462-DE2CC4DB-6387-4214-BF7A-E755B2EBDA27
Q34064462-DE2CC4DB-6387-4214-BF7A-E755B2EBDA27
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34064462-DE2CC4DB-6387-4214-BF7A-E755B2EBDA27
Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome.
P2860
Q34064462-DE2CC4DB-6387-4214-BF7A-E755B2EBDA27
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34064462-DE2CC4DB-6387-4214-BF7A-E755B2EBDA27
rank
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wasDerivedFrom
9eb0304da244426e963ab7e5bbb14e8c25dd6dd9
P2860
A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).