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Defective glutamate and K(+) clearance by cortical astrocytes in familial hemiplegic migraine type 2
Migraine is a common disabling brain disorder. A subtype of migraine with aura (familial hemiplegic migraine type 2: FHM2) is caused by loss‐of‐function mutations in α(2) Na(+),K(+) ATPase (α(2) NKA), an isoform almost exclusively expressed in astrocytes in adult brain. Cortical spreading depression...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967947/ https://www.ncbi.nlm.nih.gov/pubmed/27354390 http://dx.doi.org/10.15252/emmm.201505944 |