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Q35924271-51E452BD-200F-4B6F-B9FE-20F6A6983A20
Q35924271-51E452BD-200F-4B6F-B9FE-20F6A6983A20
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http://www.wikidata.org/entity/statement/Q35924271-51E452BD-200F-4B6F-B9FE-20F6A6983A20
Complete mitochondrial DNA sequence analysis in two southern Chinese pedigrees with Leber hereditary optic neuropathy revealed secondary mutations along with the primary mutation.
P2860
Q35924271-51E452BD-200F-4B6F-B9FE-20F6A6983A20
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35924271-51E452BD-200F-4B6F-B9FE-20F6A6983A20
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9f196f9b45a7eec2252b82cc3320d9c30bf8ff6c
P2860
Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation.