Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA.

Qiao, Chen

Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA. [electronic resource] - Molecular medicine reports Aug 2015 - 3067-72 p. digital

Publication Type: Journal Article

1791-3004

10.3892/mmr.2015.3714 doi


Adolescent
Aged
Asian People--genetics
Child
DNA Mutational Analysis
DNA, Mitochondrial--analysis
Female
Haplotypes
Humans
Male
Middle Aged
Mitochondria--genetics
Optic Atrophy, Hereditary, Leber--genetics
Pedigree
Polymorphism, Single Nucleotide