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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...
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| Gepubliceerd in: | Sci Rep |
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| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Nature Publishing Group UK
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6240030/ https://ncbi.nlm.nih.gov/pubmed/30446731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-35285-8 |
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