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

Tan AH 1 , Ozelius LJ 2 , Brashear A 3 , Lang AE 4 , Ahmad-Annuar A 1 , Tan CT 1 Show all authors , Lim SY 1

Affiliations 

  • 1 Division of Neurology and the Mah Pooi Soo & Tan Chin Nam Centre for Parkinson's & Related Disorders; and the Department of Biomedical Science Faculty of Medicine University of Malaya Kuala Lumpur Malaysia
  • 2 Departments of Genetics and Genomic Sciences and Neurology Mount Sinai School of Medicine New York New York USA
  • 3 Department of Neurology Wake Forest University School of Medicine Winston-Salem North Carolina USA
  • 4 Morton and Gloria Shulman Movement Disorders Center Toronto Western Hospital and the Edmond J. Safra Program in Parkinson's Disease Research University of Toronto Toronto Ontario Canada
Mov Disord Clin Pract, 2015 Mar;2(1):74-75.
PMID: 30713883 DOI: 10.1002/mdc3.12122

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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