Condition: Familial Hemiplegic Migraine
rs149144720 in
ATP1A2 gene and
Familial Hemiplegic Migraine
PMID 24921013 2014 Functional analysis of human Na(+)/K(+)-ATPase familial or sporadic hemiplegic migraine mutations expressed in Xenopus oocytes.
PMID 20837964 2010 De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine.
PMID 19874388 2009 Familial hemiplegic migraine is associated with febrile seizures in an FHM2 family with a novel de novo ATP1A2 mutation.
PMID 21352219 2011 Prolonged sporadic hemiplegic migraine associated with a novel de novo missense ATP1A2 gene mutation.