Table 1 Analysis of mitochondrial DNA mutations in 145 Korean probands with Leber’s hereditary optic neuropathy.

From: Mitochondrial DNA mutations in Korean patients with Leber’s hereditary optic neuropathy

 

Gene locus

Mutation

No. of probands (%)

Primary

MT-ND1

C3460A

5 (3.4)

MT-ND1

G3635A28

1 (0.7)

MT-ND1

G3733A29

1 (0.7)

MT-ND1

C4171A3

1 (0.7)

MT-ND4

G11778A

101 (69.6)

MT-ND5

G13051A30

1 (0.7)

MT-ND6

T14484C

31 (21.4)

Secondary

MT-ND1

T3394C23

2 (1.4)

MT-ND1

T3472C20

1 (0.7)

MT-ND5

G13259A21

1 (0.7)

Total

  

145

  1. MT-ND mitochondrial encoded NADH dehydrogenase.
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