ATP1A3 mutations: what is the phenotype?

Neurology. 2014 Feb 11;82(6):468-9. doi: 10.1212/WNL.0000000000000113. Epub 2014 Jan 15.

Authors

Allison Brashear¹, Laurie J Ozelius, Kathleen J Sweadner

Affiliation

¹ From the Department of Neurology (A.B.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; the Department of Genetics & Genomic Sciences (L.J.O.), Icahn School of Medicine at Mount Sinai, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Boston.

PMID: 24431297
DOI: 10.1212/WNL.0000000000000113

No abstract available

Publication types

Editorial
Comment

MeSH terms

Female
Hemiplegia / genetics*
Humans
Male
Motor Skills Disorders / genetics*
Respiratory Paralysis / genetics*
Sodium-Potassium-Exchanging ATPase / genetics*
Status Epilepticus / genetics*

Substances

ATP1A3 protein, human
Sodium-Potassium-Exchanging ATPase

Supplementary concepts

Alternating hemiplegia of childhood

Grants and funding

R01 NS058949/NS/NINDS NIH HHS/United States