Table 3 of
Miranda, Mol Vis 2016; 22:1024-1035.
Table 3. LHON mutations and haplogroups found in patients with optic neuropathy of unknown etiology (Group2).
| Mutation | Cases | Percentage | Haplogroups |
|---|---|---|---|
| G11778A | 9/34 | 26.4% | L1/L2 (3) - L3 (3) - U (1) - C (1) - D (1) |
| T14484C | 3/34 | 8.8% | L1/L2 (1) - L3 (1) - U (1) |
| G3460A | 0/34 | - | - |
| G3733A | 0/34 | - | - |
| C4171A | 0/34 | - | - |
| T10663C | 0/34 | - | - |
| G14459A | 0/34 | - | - |
| C14482G | 0/34 | - | - |
| C14482A | 0/34 | - | - |
| A14495G | 0/34 | - | - |
| C14568T | 0/34 | - | - |
| No mutation | 22/34 | 64.7% | L1/L2 (5) - L3 (9) - R (4) - H (2) T (1) - K (1) |