ATP1A3 Mutation in Adult Rapid-Onset Ataxia.

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Bibliographic Details
Title: ATP1A3 Mutation in Adult Rapid-Onset Ataxia.
Authors: Sweadner KJ; Departments of Neurosurgery, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States of America., Toro C; NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, NIH, and Office of the Clinical Director, NHGRI, Bethesda, Maryland, United States of America., Whitlow CT; Departments of Radiology and Biomedical Engineering, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America., Snively BM; Department of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America., Cook JF; Department of Neurology, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America., Ozelius LJ; Department of Neurology, Massachusetts General Hospital, Boston Massachusetts, United States of America., Markello TC; 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., Brashear A; Department of Neurology, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America.
Source: PloS one [PLoS One] 2016 Mar 18; Vol. 11 (3), pp. e0151429. Date of Electronic Publication: 2016 Mar 18 (Print Publication: 2016).
Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1932-6203
DOI:10.1371/journal.pone.0151429