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Q39951345-1961831E-D7A8-4329-9840-6A4CD1B1BD39
Q39951345-1961831E-D7A8-4329-9840-6A4CD1B1BD39
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Statement
http://www.wikidata.org/entity/statement/Q39951345-1961831E-D7A8-4329-9840-6A4CD1B1BD39
Advances in molecular diagnostics for mitochondrial diseases.
P2860
Q39951345-1961831E-D7A8-4329-9840-6A4CD1B1BD39
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39951345-1961831E-D7A8-4329-9840-6A4CD1B1BD39
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wasDerivedFrom
54a6151662ebf10c44849ed9be2c1000b3862f61
P2860
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.