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Q34366678-023A6A0F-A6E9-4401-9CD8-A0B1D4A8A252
Q34366678-023A6A0F-A6E9-4401-9CD8-A0B1D4A8A252
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34366678-023A6A0F-A6E9-4401-9CD8-A0B1D4A8A252
Mitochondrial defects in neurodegenerative disease.
P2860
Q34366678-023A6A0F-A6E9-4401-9CD8-A0B1D4A8A252
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34366678-023A6A0F-A6E9-4401-9CD8-A0B1D4A8A252
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wasDerivedFrom
4642d66ec252bec23985a773145549da97c5a8c1
P2860
Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia.