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Q33690163-3E7FDFDE-40FC-4592-8009-AEA1911C4A9D
Q33690163-3E7FDFDE-40FC-4592-8009-AEA1911C4A9D
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http://www.wikidata.org/entity/statement/Q33690163-3E7FDFDE-40FC-4592-8009-AEA1911C4A9D
Novel recessive mutations in COQ4 cause severe infantile cardiomyopathy and encephalopathy associated with CoQ10 deficiency.
P2860
Q33690163-3E7FDFDE-40FC-4592-8009-AEA1911C4A9D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33690163-3E7FDFDE-40FC-4592-8009-AEA1911C4A9D
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120440b701c93d35be7e5fa30ba35543a8ae0741
P2860
The COQ2 genotype predicts the severity of coenzyme Q10 deficiency