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Published in 2018 at "Scientific Reports"
DOI: 10.1038/s41598-018-35285-8
Abstract: 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…
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Keywords:
fhm2;
increased susceptibility;
epileptiform activity;
mouse model ... See more keywords