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...

Descrición completa

Gardado en:
Detalles 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: Society for Neuroscience 2011
Assuntos:
Articles
Acceso en liña: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: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares