Brief Report with Video
Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: Clinical implications
Article first published online: 11 JUN 2004
Copyright © 2004 Movement Disorder Society
Volume 19, Issue 11, pages 1357–1360, November 2004
How to Cite
Shan, D.-E., Liu, R.-S., Sun, C.-M., Lee, S.-J., Liao, K.-K. and Soong, B.-W. (2004), Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: Clinical implications. Mov. Disord., 19: 1357–1360. doi: 10.1002/mds.20212
- Issue published online: 18 OCT 2004
- Article first published online: 11 JUN 2004
- Manuscript Accepted: 27 MAR 2004
- Manuscript Revised: 8 MAR 2004
- Manuscript Received: 20 JAN 2004
- National Science Council, ROC. Grant Numbers: NSC-91-2314-B-075-045, NSC 90-2314-B-010-028
- Taipei Veterans General Hospital. Grant Numbers: VGH-90-372, VGH-92-308
- VTY Joint Research Program, Tsou's Foundation. Grant Number: VTY92-P5-39
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