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

Lancet

Volumn 352, Issue 9126, 1998, Pages 455-456

  Majamaa, Kari ^a   Finnilä, Saara ^a   Turkka, Jukka ^a   Hassinen, Ilmo E ^a  

^a UNIVERSITY OF OULU   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; ARTICLE; CLINICAL ARTICLE; FEMALE; GENOTYPE; HUMAN; MALE; MELAS SYNDROME; MIGRAINE; OCCIPITAL LOBE; POINT MUTATION; PRIORITY JOURNAL; RISK FACTOR; STROKE;

EID: 0032497128     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(05)79190-X     Document Type: Article

References (5)

1. 1 Shoffner JM. Maternal inheritance and the evaluation of oxidative phosphorylation diseases. Lancet 1996; 348: 1283-88.
2. 2 Majamaa K, Turkka J, Kärppä M, Winqvist S, Hassien IE. The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brian infarct. Neurology 1997; 49: 1331-34.
3. 3 Klopstock T, May A, Seibel P, Papagiannuli E, Diener HC, Reichmann H. Mitochondrial DNA in migraine with aura. Neurology 1996; 46: 1735-38.
4. 4 Johnson CJ, Kittner SJ, McCarter RJ, et al. Interrater reliability of an etiologic classification of ischemic stroke. Stroke 1995; 26: 46-51.
5. 5 Torroni A, Huoponen K, Francalacci P, et al. Classification of European mtDNAs from an analysis of three European populations. Genetics 1996; 144: 1835-50.