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

Background. The LRRK2 G2019S mutation is the most common genetic determinant of Parkinson's disease (PD) identified to date. This mutation, reported in both familial and sporadic PD, occurs at elevated frequencies in Maghreb population. In the present study, we examined the prevalence of the G2...

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Detalhes bibliográficos
Publicado no:Parkinsons Dis
Main Authors: Bouhouche, Ahmed, Tibar, Houyam, Ben El Haj, Rafiqua, El Bayad, Khalil, Razine, Rachid, Tazrout, Sanaa, Skalli, Asmae, Bouslam, Naima, Elouardi, Loubna, Benomar, Ali, Yahyaoui, Mohammed, Regragui, Wafa
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2017
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5390546/
https://ncbi.nlm.nih.gov/pubmed/28465860
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/2412486
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