Rapid‐Onset Dystonia‐Parkinsonism in a Chinese Girl with a De Novo ATP1A3 c.2267G>A (p.R756H) Genetic Mutation

समान संसाधन

• Revising Rapid-Onset Dystonia-Parkinsonism: broadening indications for ATP1A3 testing
  द्वारा: Haq, Ihtsham U., और अन्य
  प्रकाशित: (2019)
• Genotype-structure-phenotype relationships diverge in paralogs ATP1A1, ATP1A2, and ATP1A3
  द्वारा: Sweadner, Kathleen J., और अन्य
  प्रकाशित: (2019)
• ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia
  द्वारा: BRASHEAR, ALLISON, और अन्य
  प्रकाशित: (2012)
• Genetics in Dystonia: An Update
  द्वारा: Fuchs, Tania, और अन्य
  प्रकाशित: (2013)
• Alternating Hemiplegia of Childhood in a Person of Malay Ethnicity with Diffusion Tensor Imaging Abnormalities
  द्वारा: Tan, Ai Huey, और अन्य
  प्रकाशित: (2019)