Increased Susceptibility to Cortical Spreading Depression in the Mouse Model of Familial Hemiplegic Migraine Type 2

Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant form of migraine with aura that is caused by mutations of the α2-subunit of the Na,K-ATPase, an isoform almost exclusively expressed in astrocytes in the adult brain. We generated the first FHM2 knock-in mouse model carrying the hum...

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Detalles Bibliográficos
Autores principales: Leo, Loredana, Gherardini, Lisa, Barone, Virginia, De Fusco, Maurizio, Pietrobon, Daniela, Pizzorusso, Tommaso, Casari, Giorgio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121757/
https://www.ncbi.nlm.nih.gov/pubmed/21731499
http://dx.doi.org/10.1371/journal.pgen.1002129

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121757/
https://www.ncbi.nlm.nih.gov/pubmed/21731499
http://dx.doi.org/10.1371/journal.pgen.1002129

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