Analysis of Genetic Variants in SCN1A, SCN2A, KCNK18, TRPA1 and STX1A as a Possible Marker of Migraine

BACKGROUND: Migraine is a polygenetic disease, considered as a channelopathy. The dysregulation of ion functioning due to genetic changes may activate the trigeminovascular system and induce migraine attack both migraine with aura (MA) and without aura (MO). OBJECTIVES: The aim of the study was to a...

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Detalles Bibliográficos
Autores principales: Kowalska, Marta, Prendecki, Michał, Kapelusiak-Pielok, Magdalena, Grzelak, Teresa, Łagan-Jędrzejczyk, Urszula, Wiszniewska, Małgorzata, Kozubski, Wojciech, Dorszewska, Jolanta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521035/
https://www.ncbi.nlm.nih.gov/pubmed/33071616
http://dx.doi.org/10.2174/1389202921666200415181222

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521035/
https://www.ncbi.nlm.nih.gov/pubmed/33071616
http://dx.doi.org/10.2174/1389202921666200415181222

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