IndraLab

Statements

sparser
"We extracted the genetic profiles of ATP1A2 , CACNA1A , SCN1A , and PRRT2 associated with FHM from our statistical results ( xref in the online-only Data Supplement), and identified five variants in ATP1A2 and CACNA1A that were significantly associated with the all-migraine group ( p <0.05)."
38951977
sparser
"Mutations in the CACNA1A and ATP1A2 genes are associated with familial hemiplegic migraine, a rare subtype of migraine with aura ."
16356649
sparser
"This disease has been associated with missense mutations in the CACNA1A and ATP1A2 genes."
17119788