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Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine https://t.co/N4Rqis0YVs
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New Research: Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine: Familial hemiplegic migraine (FHM) is a severe neurogenetic disorder for which three causal genes, CACNA1A, SCN1A, and ATP1A2, have been… https://t.co/Ih0IXljmgs #Molecular #