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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...
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| Publicado no: | EMBO Mol Med |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4967947/ https://ncbi.nlm.nih.gov/pubmed/27354390 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/emmm.201505944 |
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