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Q34007681-74718E74-C331-46FB-BBD9-445F4F05DE52
Q34007681-74718E74-C331-46FB-BBD9-445F4F05DE52
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Statement
http://www.wikidata.org/entity/statement/Q34007681-74718E74-C331-46FB-BBD9-445F4F05DE52
Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.
P2860
Q34007681-74718E74-C331-46FB-BBD9-445F4F05DE52
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34007681-74718E74-C331-46FB-BBD9-445F4F05DE52
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wasDerivedFrom
4990152b2f9735d22d74e18fed3e981e6050c6c3
P2860
Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.