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Q33690163-2FE45A59-D03F-45C6-A269-F1C5DC5E5E7C
Q33690163-2FE45A59-D03F-45C6-A269-F1C5DC5E5E7C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33690163-2FE45A59-D03F-45C6-A269-F1C5DC5E5E7C
Novel recessive mutations in COQ4 cause severe infantile cardiomyopathy and encephalopathy associated with CoQ10 deficiency.
P2860
Q33690163-2FE45A59-D03F-45C6-A269-F1C5DC5E5E7C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33690163-2FE45A59-D03F-45C6-A269-F1C5DC5E5E7C
rank
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type
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Statement
wasDerivedFrom
120440b701c93d35be7e5fa30ba35543a8ae0741
P2860
Human coenzyme Q10 deficiency