IndraLab

Statements

CACNA1A activates FHM. 2 / 2
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"We now report on a mutation identified in the first intracellular loop of CACNA1A (alpha (1A (A454T))) that does not cause FHM but is associated with the absence of sensorimotor symptoms in a migraine with aura pedigree."
20080591
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"XREF_BIBR Rare mutations in the CACNA1A, ATP1A2 and SCN1A genes can all cause FHM, revealing genetic heterogeneity in the disorder."
31980564