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Q34450113-554FD02D-BEC4-4895-BEE5-78C4351FB425
Q34450113-554FD02D-BEC4-4895-BEE5-78C4351FB425
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Statement
http://www.wikidata.org/entity/statement/Q34450113-554FD02D-BEC4-4895-BEE5-78C4351FB425
Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy
P2860
Q34450113-554FD02D-BEC4-4895-BEE5-78C4351FB425
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34450113-554FD02D-BEC4-4895-BEE5-78C4351FB425
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wasDerivedFrom
55ca349d2bf63438764d316978b8b8c7d1d77481
P2860
MTO1 mutations are associated with hypertrophic cardiomyopathy and lactic acidosis and cause respiratory chain deficiency in humans and yeast.