Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln

被引:26
作者
Finnilä, S
Autere, J
Lehtovirta, M
Hartikainen, P
Mannermaa, A
Soininen, H
Majamaa, K
机构
[1] Univ Oulu, Dept Neurol, FIN-90014 Oulu, Finland
[2] Univ Oulu, Dept Med Biochem, Oulu, Finland
[3] Univ Oulu, Bioctr, Oulu, Finland
[4] Univ Kuopio, Dept Neurol, FIN-70211 Kuopio, Finland
[5] Kuopio Univ Hosp, DNA & Chromosome Lab, SF-70210 Kuopio, Finland
关键词
D O I
10.1136/jmg.38.6.400
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:400 / 405
页数:6
相关论文
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