ATP1A3 Mutations and Genotype-Phenotype Correlation of Alternating Hemiplegia of Childhood in Chinese Patients

Author:

Yang Xiaoling,Gao Hua,Zhang Jie,Xu Xiaojing,Liu Xiaoyan,Wu Xiru,Wei Liping,Zhang Yuehua

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference40 articles.

1. The treatment and management of alternating hemiplegia of childhood;BG Neville;Dev Med Child Neurol,2007

2. De novo mutations in ATP1A3 cause alternating hemiplegia of childhood;EL Heinzen;Nat Genet,2012

3. The multiple faces of the ATP1A3-related dystonic movement disorder;A Roubergue;Mov Disord,2013

4. Alternating hemiplegia of childhood;M Bourgeois;J Pediatr,1993

5. Alternating hemiplegia in childhood: a report of eight patients with complicated migraine beginning in infancy;S Verret;Pediatrics,1971

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