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Q40546537-751222CC-FCE2-4C66-983C-E6696FB85FDA
Q40546537-751222CC-FCE2-4C66-983C-E6696FB85FDA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40546537-751222CC-FCE2-4C66-983C-E6696FB85FDA
Mitochondrial encephalomyopathy with autosomal dominant inheritance: a clinical and genetic entity of mitochondrial diseases.
P2860
Q40546537-751222CC-FCE2-4C66-983C-E6696FB85FDA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q40546537-751222CC-FCE2-4C66-983C-E6696FB85FDA
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
092a613b22ea8740834381bbbba3b8172044b995
P2860
Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle.