
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).
DOI: https://doi.org/10.15844/pedneurbriefs-28-4-8 | Journal eISSN: 2166-6482
Language: English
Page range: 31 - 31
Published on: Apr 1, 2014
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2014 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.