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Q26770152-35C1C14A-E51D-43B6-A77A-7B33A224CDCC
Q26770152-35C1C14A-E51D-43B6-A77A-7B33A224CDCC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26770152-35C1C14A-E51D-43B6-A77A-7B33A224CDCC
Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease
P2860
Q26770152-35C1C14A-E51D-43B6-A77A-7B33A224CDCC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q26770152-35C1C14A-E51D-43B6-A77A-7B33A224CDCC
rank
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Statement
wasDerivedFrom
5ec9ba8751f5caf255e46e26f5b94bdbcc4e36c0
P2860
A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia