Potential conflict of interest: Nothing to report.
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa
Version of Record online: 18 AUG 2010
Copyright © 2010 Movement Disorder Society
Volume 25, Issue 13, pages 2052–2058, 15 October 2010
How to Cite
Jasinska-Myga, B., Kachergus, J., Vilariño-Güell, C., Wider, C., Soto-Ortolaza, A. I., Kefi, M., Middleton, L. T., Ishihara-Paul, L., Gibson, R. A., Amouri, R., Yahmed, S. B., Sassi, S. B., Zouari, M., Euch, G. E., Ross, O. A., Hentati, F. and Farrer, M. J. (2010), Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa. Mov. Disord., 25: 2052–2058. doi: 10.1002/mds.23283
- Issue online: 7 OCT 2010
- Version of Record online: 18 AUG 2010
- Manuscript Accepted: 10 MAY 2010
- Manuscript Revised: 27 DEC 2009
- Manuscript Received: 4 SEP 2009
- The Neurogenetic Core of the Mayo Clinic Morris K. Udall Center. Grant Number: NINDS P50 NS40256
- The Medical University of Silesia, Poland
- The Polish Foundation for Development of Neurology, Degenerative and Cerebrovascular Diseases.
- The Swiss National Science Foundation. Grant Number: PASMP3-123268
- The Morris K. Udall Center of Excellence for Parkinson's Disease Research. Grant Number: NS40256
- The National Institutes of Health Exploratory/Developmental Research Grant Award. Grant Number: R21 NS64885
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