Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine

被引:53
作者
Majamaa, K
Finnilä, S
Turkka, J
Hassinen, IE
机构
[1] Oulu Univ, Dept Neurol, FIN-90220 Oulu, Finland
[2] Oulu Univ, Dept Biochem Med, FIN-90220 Oulu, Finland
基金
芬兰科学院;
关键词
D O I
10.1016/S0140-6736(05)79190-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:455 / 456
页数:2
相关论文
共 5 条
[1]   INTERRATER RELIABILITY OF AN ETIOLOGIC CLASSIFICATION OF ISCHEMIC STROKE [J].
JOHNSON, CJ ;
KITTNER, SJ ;
MCCARTER, RJ ;
SLOAN, MA ;
STERN, BJ ;
BUCHHOLZ, D ;
PRICE, TR .
STROKE, 1995, 26 (01) :46-51
[2]   Mitochondrial DNA in migraine with aura [J].
Klopstock, T ;
May, A ;
Seibel, P ;
Papagiannuli, E ;
Diener, HC ;
Reichmann, H .
NEUROLOGY, 1996, 46 (06) :1735-1738
[3]   The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct [J].
Majamaa, K ;
Turkka, J ;
Karppa, M ;
Winqvist, S ;
Hassinen, IE .
NEUROLOGY, 1997, 49 (05) :1331-1334
[4]   Maternal inheritance and the evaluation of oxidative phosphorylation diseases [J].
Shoffner, JM .
LANCET, 1996, 348 (9037) :1283-1288
[5]  
Torroni A, 1996, GENETICS, V144, P1835