Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.

Biochemistry, Genetics and Molecular Biology

• Mutation 100%
• ATP1A3 46%
• Nested Gene 26%
• Phenotype 26%
• Spectrum 13%
• Childhood 13%
• Genotype Phenotype Correlation 6%
• Age 6%
• Clinical Trial 6%