Genotype-Phenotype Correlations in Alternating Hemiplegia

Abstract

Researchers at the National Center of Neurology and Psychiatry, Kodaira, and multiple centers in Japan, analyze the clinical features and ATP1A3 mutations in 35 Japanese children diagnosed with alternating hemiplegia of childhood (AHC).

Keywords

• alternating hemiplegia
• sodium-potassium-atpase
• genotype-phenotype