Table of Contents Author Guidelines Submit a Manuscript
Parkinson’s Disease
Volume 2017, Article ID 2412486, 7 pages
https://doi.org/10.1155/2017/2412486
Research Article

LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease

1Research Team in Neurology and Neurogenetics, Medical School and Pharmacy, Mohammed V University, Rabat, Morocco
2Department of Neurology and Neurogenetics, Specialties Hospital, Rabat, Morocco
3Laboratory of Public Health, Medical School and Pharmacy, Mohammed V University, Rabat, Morocco

Correspondence should be addressed to Ahmed Bouhouche; am.ten.s5mu@ehcuohuob.a

Received 9 December 2016; Accepted 23 March 2017; Published 30 March 2017

Academic Editor: Daniel Berwick

Copyright © 2017 Ahmed Bouhouche et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Ahmed Bouhouche, Houyam Tibar, Rafiqua Ben El Haj, et al., “LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease,” Parkinson’s Disease, vol. 2017, Article ID 2412486, 7 pages, 2017. https://doi.org/10.1155/2017/2412486.