Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.

Sudoyo, Herawati

Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy. [electronic resource] - Journal of human genetics 2002 - 594-604 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1434-5161

10.1007/s100380200091 doi


Asia, Southeastern--epidemiology
DNA, Mitochondrial
Female
Haplotypes
Humans
Male
Mitochondria--genetics
Mutation
Optic Atrophy, Hereditary, Leber--epidemiology
Phylogeny
Polymorphism, Single Nucleotide