Table 2 Relative frequency of the three primary mutations confirmed among different populations.
From: Mitochondrial DNA mutations in Korean patients with Leber’s hereditary optic neuropathy
Population | G11778A (%) | T14484C (%) | G3460A (%) | Other primary mutations |
|---|---|---|---|---|
Northern Europe, UK, Australia2 | 69 | 14 | 13 | |
Finland5 | 79 | 4 | 17 | |
Denmark6 | 67 | 18 | 13 | A3395G |
France7 | 72 | 12 | 16 | |
Italian8 | 66 | 16 | 18 | |
The US9 | 49 | 23 | 28 | |
India (North)10 | 100* | 9* | Nil | |
India (South)11 | 90 | 7 | Nil | C4171A T12338C |
India12 | 85 | 13 | 2 | |
China (Han)13 | 86 | 13 | 1 | |
Taiwan14 | 92 | 8 | Nil | |
Japan15 | 87 | 9 | 4 | |
Japan16 | 87 | 11 | 2 | |
Japan17 | 82 | 15 | Nil | G11696A T12811C |
Korea18 | 76 | 22 | 2 | |
Korea19 | 87 | 13 | Nil | |
Present study | 69 | 21 | 3 | G3635A G3733A C4171A G13051A |