ATP1A2

Publications

De Fusco M et al. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2. Nat Genet. 2003;33(2):192-6.  PMID: 12539047.

Vanmolkot K R et al. Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. Ann Neurol. 2003;54(3):360-6.  PMID: 12953268.

Vanmolkot K R et al. Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine. Eur J Hum Genet. 2006;14(5):555-60.  PMID: 16538223.

Vanmolkot K R et al. First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine. Eur J Hum Genet. 2007;15(8):884-8.  PMID: 17473835.

Pelzer N et al. Familial hemiplegic migraine treated by sodium valproate and lamotrigine. Cephalalgia. 2014;34(9):708-711.  PMID: 24443394.

Isaksen T J et al. Insights into the Pathology of the α2-Na(+)/K(+)-ATPase in Neurological Disorders; Lessons from Animal Models. Front Physiol. 2016;7:161.  PMID 27199775.

Friedrich T et al. ATP1A2 Mutations in Migraine: Seeing through the Facets of an Ion Pump onto the Neurobiology of Disease. Front Physiol. 2016;7:239.  PMID 27445835.

Pelzer N et al. Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation. Neurology. 2018;90(7):e575-e582.  PMID: 29343472.