Chromosome 19p13 Loci in Finnish Migraine With Aura Families

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 (FHM1). Contribution of CACN...

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Bibliografski detalji
Izdano u:Am J Med Genet B Neuropsychiatr Genet
Glavni autori: Kaunisto, Mari A., Tikka, Päivi J., Kallela, Mikko, Leal, Suzanne M., Papp, Jeanette C., Korhonen, Arja, Hämäläinen, Eija, Harno, Hanna, Havanka, Hannele, Nissilä, Markku, Säkö, Erkki, Ilmavirta, Matti, Kaprio, Jaakko, Färkkilä, Markus, Ophoff, Roel A., Palotie, Aarno, Wessman, Maija
Format: Artigo
Jezik:Inglês
Izdano: 2005
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Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6217809/
https://ncbi.nlm.nih.gov/pubmed/15449251
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.30082
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