Enhanced Subcortical Spreading Depression in Familial Hemiplegic Migraine Type 1 Mutant Mice

Familial hemiplegic migraine type 1, a monogenic migraine variant with aura, is linked to gain-of-function mutations in the CACNA1A gene encoding Ca(V)2.1 channels. The S218L mutation causes severe channel dysfunction, and paroxysmal migraine attacks can be accompanied by seizures, coma, and hemiple...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Eikermann-Haerter, Katharina, Yuzawa, Izumi, Qin, Tao, Wang, Yumei, Baek, Kwangyeol, Kim, Young Ro, Hoffmann, Ulrike, Dilekoz, Ergin, Waeber, Christian, Ferrari, Michel D., van den Maagdenberg, Arn M. J. M., Moskowitz, Michael A., Ayata, Cenk
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2011
Assuntos:
Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3135337/
https://ncbi.nlm.nih.gov/pubmed/21490217
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.5346-10.2011
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados