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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390546/ https://www.ncbi.nlm.nih.gov/pubmed/28465860 http://dx.doi.org/10.1155/2017/2412486 |