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Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1
Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden.
Linköping University, Faculty of Health Sciences. Linköping University, Department of Clinical and Experimental Medicine, Psychiatry .
Umea Univ, Umea Ctr Mol Med, Umea, Sweden Umea Univ, Dept Neurol, S-90187 Umea, Sweden Umea Univ, Dept Med Biosci Clin Genet, Umea, Sweden Linkoping Univ, Dept Neurosci & Locomot, Linkoping, Sweden Kalmar Hosp, Dept Psychiat, Kalmar, Sweden.
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2002 (English)In: Neurology, ISSN 0028-3878, E-ISSN 1526-632X, Vol. 59, no 11, 1804-1807 p.Article in journal (Refereed) Published
Abstract [en]

Migraine is the most common type of chronic episodic headache. To find novel susceptibility genes for familial migraine with and without aura, a genomewide screen was performed in a large family from northern Sweden. Evidence of linkage was obtained on chromosome 6p12.2-p21.1, with a maximum two-point lod score of 5.41 for marker D6S452. The patients with migraine shared a common haplotype of 10 Mb between markers D6S1650 and D6S1960.

Place, publisher, year, edition, pages
2002. Vol. 59, no 11, 1804-1807 p.
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Medical and Health Sciences
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URN: urn:nbn:se:liu:diva-48709OAI: oai:DiVA.org:liu-48709DiVA: diva2:269605
Available from: 2009-10-11 Created: 2009-10-11 Last updated: 2017-12-12

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Nylander, Per-Olof

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