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Allele Publication :

Type  Indexed Publication . Mgi Jnum  J:321889
Publication . Citation  Terpollili NA, et al. (2022) CaV2.1 channel mutations causing familial hemiplegic migraine type 1 increase the susceptibility for cortical spreading depolarizations and seizures and worsen outcome after experimental traumatic brain injury. Elife 11:e74923
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