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Q24645475-49DA51C0-7B1B-4112-ADA8-FCA7F70FE0BD
Q24645475-49DA51C0-7B1B-4112-ADA8-FCA7F70FE0BD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24645475-49DA51C0-7B1B-4112-ADA8-FCA7F70FE0BD
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease
P2860
Q24645475-49DA51C0-7B1B-4112-ADA8-FCA7F70FE0BD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24645475-49DA51C0-7B1B-4112-ADA8-FCA7F70FE0BD
rank
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type
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wasDerivedFrom
ea785166b92f99b41c90a393e05a11795284fde1
P2860
Prenyldiphosphate synthase, subunit 1 (PDSS1) and OH-benzoate polyprenyltransferase (COQ2) mutations in ubiquinone deficiency and oxidative phosphorylation disorders