Potential conflict of interest: None reported.
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations†
Article first published online: 9 FEB 2009
Copyright © 2009 Movement Disorder Society
Volume 24, Issue 5, pages 662–666, 15 April 2009
How to Cite
Camargos, S. T., Dornas, L. O., Momeni, P., Lees, A., Hardy, J., Singleton, A. and Cardoso, F. (2009), Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations. Mov. Disord., 24: 662–666. doi: 10.1002/mds.22365
- Issue published online: 24 APR 2009
- Article first published online: 9 FEB 2009
- Manuscript Accepted: 24 SEP 2008
- Manuscript Revised: 4 AUG 2008
- Manuscript Received: 18 FEB 2008
- Intramural Research Program of the National Institute on Aging
- National Institutes of Health
- Department of Health and Human Services
- NIH. Grant Number: Z01 AG000957-05
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