From: Mitochondrial DNA variant m.15218A > G in Finnish epilepsy patients who have maternal relatives with epilepsy, sensorineural hearing impairment or diabetes mellitus
Patients
Controls1
Haplogroup
(N)
(%)
H
32
25.3
162
40.1
U
21
16.6
112
27.8
V
7
5.5
22
5.4
W
5
3.9
37
9.2
J
4
3.2
18
4.4
K
3
2.4
12
2.9
T
10
2.5
I
2
1.6
14
3.5
X
0.9
M
0
Other
1
0.2