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haplogroup (3) 3
humans (3) 3
index medicus (3) 3
lhon (3) 3
mutations (3) 3
ophthalmology (3) 3
pedigree (3) 3
adult (2) 2
clinical expression (2) 2
dna (2) 2
dna, mitochondrial - genetics (2) 2
female (2) 2
gene (2) 2
haplotypes (2) 2
male (2) 2
mtdna (2) 2
nadh dehydrogenase - genetics (2) 2
optic atrophy, hereditary, leber - genetics (2) 2
optic atrophy, hereditary, leber - pathology (2) 2
penetrance (2) 2
young adult (2) 2
asian continental ancestry group - genetics (1) 1
disease (1) 1
dna mutational analysis (1) 1
dna, mitochondrial (1) 1
epidemiology (1) 1
evolution, molecular (1) 1
families (1) 1
family (1) 1
family health (1) 1
g11778a mutation (1) 1
genetic heterogeneity (1) 1
han chinese families (1) 1
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haplotypes - genetics (1) 1
hereditary optic neuropathy (1) 1
human mitochondrial genome (1) 1
identification (1) 1
india (1) 1
india - epidemiology (1) 1
lhon patients (1) 1
life sciences (1) 1
low penetrance (1) 1
m. 11778g>a (1) 1
m.11778g>a (1) 1
m.14484t > c (1) 1
m.14484t>c (1) 1
mitochondria - genetics (1) 1
mutation (1) 1
optic atrophy, hereditary, leber (1) 1
optic atrophy, hereditary, leber - epidemiology (1) 1
optic atrophy, hereditary, leber - ethnology (1) 1
pedigrees (1) 1
phenotypic manifestation (1) 1
phylogeny (1) 1
point mutation (1) 1
point mutation - genetics (1) 1
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