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Q33690163-8848C9F2-7D8E-44E2-A7DA-122E188C79BC
Q33690163-8848C9F2-7D8E-44E2-A7DA-122E188C79BC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33690163-8848C9F2-7D8E-44E2-A7DA-122E188C79BC
Novel recessive mutations in COQ4 cause severe infantile cardiomyopathy and encephalopathy associated with CoQ10 deficiency.
P2860
Q33690163-8848C9F2-7D8E-44E2-A7DA-122E188C79BC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33690163-8848C9F2-7D8E-44E2-A7DA-122E188C79BC
rank
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type
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Statement
wasDerivedFrom
120440b701c93d35be7e5fa30ba35543a8ae0741
P2860
Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders