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BioMed Research International
Volume 2016, Article ID 3460234, 5 pages
http://dx.doi.org/10.1155/2016/3460234
Research Article

A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism

1Research Team on Neurodegenerative Diseases, Medical School and Pharmacy, Mohammed V University, 10100 Rabat, Morocco
2Department of Neurology and Neurogenetics, Specialties Hospital, CHU Ibn Sina, 10100 Rabat, Morocco
3Laboratory of Biotechnology, Medical School and Pharmacy, Mohammed V University, 10100 Rabat, Morocco

Received 2 March 2016; Revised 4 May 2016; Accepted 16 May 2016

Academic Editor: Enza M. Valente

Copyright © 2016 Rafiqua Ben El Haj 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

Rafiqua Ben El Haj, Wafaa Regragui, Rachid Tazi-Ahnini, et al., “A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism,” BioMed Research International, vol. 2016, Article ID 3460234, 5 pages, 2016. https://doi.org/10.1155/2016/3460234.