A case of early onset life-threatening epilepsy associated with a novel ATP1A3 gene variant

Mutations in the Na+/K+-ATPase α3 Gene ATP1A3 Are Associated with Rapid-Onset Dystonia Parkinsonism

Patrícia de Carvalho Aguiar, Kathleen J. Sweadner, John T. Penniston et al. · Neuron · 2004 · 511 citations · Full text

Medicine, Genetics, Neuroscience +12

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi et al. · Nature Genetics · 2012 · 423 citations · Full text

Life Sciences, Genetics, Neurology +9

Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study

Hendrik Rosewich, Hölger Thiele, Andreas Ohlenbusch et al. · The Lancet Neurology · 2012 · 267 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

ALTERNATING HEMIPLEGIA IN CHILDHOOD: A REPORT OF EIGHT PATIENTS WITH COMPLICATED MIGRAINE BEGINNING IN INFANCY

S Verret, John C. Steele · PEDIATRICS · 1971 · 201 citations

Medicine, Neurology, Pediatrics +16

A novel recurrent mutation in ATP1A3 causes CAPOS syndrome

Michelle Demos, Clara DM van Karnebeek, Colin J.D. Ross et al. · Orphanet Journal of Rare Diseases · 2014 · 192 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17