Alternating hemiplegia of childhood (AHC) is a rare, one-in-a-million genetic disease that affects kids. Most cases are caused by mutations in the ATP1A3 gene. That gene makes an ATPase enzyme ...

ATP1A3 dysfunction causes motor hyperexcitability and afterhyperpolarization loss in a dystonia model Journal: Brain Published: 2024-11-14 DOI: 10.1093/brain/awae373 Affiliations: 10 Authors: 16 ...