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Q33793717-20183C46-5E62-4EF3-994C-A7A62A7AB06D
Q33793717-20183C46-5E62-4EF3-994C-A7A62A7AB06D
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http://www.wikidata.org/entity/statement/Q33793717-20183C46-5E62-4EF3-994C-A7A62A7AB06D
Mitochondrial disorders. A diagnostic challenge in clinical chemistry.
P2860
Q33793717-20183C46-5E62-4EF3-994C-A7A62A7AB06D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33793717-20183C46-5E62-4EF3-994C-A7A62A7AB06D
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wasDerivedFrom
ad0f3cb3039eaf684598d7bed66de5d95bbc4078
P2860
A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy.