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Q33715521-D3F2FB4B-72FF-4831-B50C-9507634735DF
Q33715521-D3F2FB4B-72FF-4831-B50C-9507634735DF
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http://www.wikidata.org/entity/statement/Q33715521-D3F2FB4B-72FF-4831-B50C-9507634735DF
Clinical and functional characterisation of the combined respiratory chain defect in two sisters due to autosomal recessive mutations in MTFMT
P2860
Q33715521-D3F2FB4B-72FF-4831-B50C-9507634735DF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33715521-D3F2FB4B-72FF-4831-B50C-9507634735DF
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wasDerivedFrom
ff9010e002af4291da1f1b6b06645675c68abd6e
P2860
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene