Chinese patients with p.Arg756 mutations of ATP1A3 : Clinical manifestations, treatment, and follow‐up
Author:
Affiliation:
1. Department of Neurology Beijing Children's Hospital, Capital Medical University, National Center for Children's Health Beijing China
Publisher
Wiley
Subject
Pediatrics, Perinatology and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ped4.12310
Reference24 articles.
1. Relapsing encephalopathy with cerebellar ataxia related to anATP1A3mutation
2. Fever-Induced Paroxysmal Weakness and Encephalopathy, a New Phenotype of ATP1A3 Mutation
3. Knock-in mouse model of alternating hemiplegia of childhood: Behavioral and electrophysiologic characterization
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