A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood

Lignende værker

• De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
  af: Heinzen, Erin L., et al.
  Udgivet: (2012)
• Treatment with Oral ATP decreases alternating hemiplegia of childhood with de novo ATP1A3 Mutation
  af: Ju, Jun, et al.
  Udgivet: (2016)
• ATP1A3 Mutations and Genotype-Phenotype Correlation of Alternating Hemiplegia of Childhood in Chinese Patients
  af: Yang, Xiaoling, et al.
  Udgivet: (2014)
• Alternating Hemiplegia of Childhood
  af: Aylward, Rebecca
  Udgivet: (1996)
• ATP1A3 mosaicism in families with alternating hemiplegia of childhood
  af: Yang, Xiaoling, et al.
  Udgivet: (2019)