ATP1A3 mutations in infants: a new rapid-onset dystonia–Parkinsonism phenotype characterized by motor delay and ataxia

✍ Scribed by ALLISON BRASHEAR; JONATHAN W MINK; DEBORAH F HILL; NIKI BOGGS; W VAUGHN MCCALL; MARK A STACY; BEVERLY SNIVELY; LANEY S LIGHT; KATHLEEN J SWEADNER; LAURIE J OZELIUS; LESLIE MORRISON

• Book ID: 117954116
• Publisher: John Wiley and Sons
• Year: 2012
• Tongue: English
• Weight: 76 KB
• Volume: 54
• Category: Article
• ISSN: 0012-1622
• DOI: 10.1111/j.1469-8749.2012.04421.x