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Q37004752-C8CDCC10-B41B-47FC-9094-BDD6E42ED956
Q37004752-C8CDCC10-B41B-47FC-9094-BDD6E42ED956
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37004752-C8CDCC10-B41B-47FC-9094-BDD6E42ED956
Mutations in the ND5 subunit of complex I of the mitochondrial DNA are a frequent cause of oxidative phosphorylation disease.
P2860
Q37004752-C8CDCC10-B41B-47FC-9094-BDD6E42ED956
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37004752-C8CDCC10-B41B-47FC-9094-BDD6E42ED956
rank
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type
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Statement
wasDerivedFrom
244f5581e4ea27d889e7c122fd4d3fa46df0e7b2
P2860
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy