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Increased susceptibility to cortical spreading depression and epileptiform activity in a mouse model for FHM2
Migraine is a highly prevalent, debilitating, episodic headache disorder affecting roughly 15% of the population. Familial hemiplegic migraine type 2 (FHM2) is a rare subtype of migraine caused by mutations in the ATP1A2 gene, encoding the α(2) isoform of the Na(+)/K(+)-ATPase, predominantly express...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Nature Publishing Group UK
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240030/ https://www.ncbi.nlm.nih.gov/pubmed/30446731 http://dx.doi.org/10.1038/s41598-018-35285-8 |