ATP1A3 Mutation in Adult Rapid-Onset Ataxia

• Kathleen J. Sweadner ,

  * E-mail: sweadner@helix.mgh.harvard.edu

  Affiliation Departments of Neurosurgery, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States of America

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• Camilo Toro,

  Affiliation NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH, and Office of the Clinical Director, NHGRI, Bethesda, Maryland, United States of America

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• Christopher T. Whitlow,

  Affiliation Departments of Radiology and Biomedical Engineering, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America

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• Beverly M. Snively,

  Affiliation Department of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America

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• Jared F. Cook,

  Affiliation Department of Neurology, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America

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• Laurie J. Ozelius,

  Affiliation Department of Neurology, Massachusetts General Hospital, Boston Massachusetts, United States of America

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• Thomas C. Markello,

  Affiliation NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH, and Human Biochemical Genetics Section, Medical Genetics Branch, NHGRI, Bethesda, Maryland, United States of America

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• Allison Brashear

  Affiliation Department of Neurology, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America

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