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Commentary to ‘Comorbidity in Finnish migraine families’

✍ Scribed by Michael Bjørn Russell

Publisher
Springer
Year
2006
Tongue
English
Weight
40 KB
Volume
7
Category
Article
ISSN
1129-2369

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## Abstract Chromosomal area 19p13 contains two migraine associated genes: a Ca~v~2.1 (P/Q‐type) calcium channel α~1~ subunit gene, __CACNA1A__, and an insulin receptor gene, __INSR__. Missense mutations in __CACNA1A__ cause a rare Mendelian form of migraine, familial hemiplegic migraine type 1 (FH