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Q33690163-5062C9F9-6F46-4892-BF54-0C17B8C2C057
Q33690163-5062C9F9-6F46-4892-BF54-0C17B8C2C057
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33690163-5062C9F9-6F46-4892-BF54-0C17B8C2C057
Novel recessive mutations in COQ4 cause severe infantile cardiomyopathy and encephalopathy associated with CoQ10 deficiency.
P2860
Q33690163-5062C9F9-6F46-4892-BF54-0C17B8C2C057
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33690163-5062C9F9-6F46-4892-BF54-0C17B8C2C057
rank
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type
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Statement
wasDerivedFrom
120440b701c93d35be7e5fa30ba35543a8ae0741
P2860
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations