Mutation Analysis of Consanguineous Moroccan Patients with Parkinson’s Disease Combining Microarray and Gene Panel

During the last two decades, 15 different genes have been reported to be responsible for the monogenic form of Parkinson’s disease (PD), representing a worldwide frequency of 5–10%. Among them, 10 genes have been associated with autosomal recessive PD, with PRKN and PINK1 being the most frequent. In...

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Detalles Bibliográficos
Autores principales: Bouhouche, Ahmed, Tesson, Christelle, Regragui, Wafaa, Rahmani, Mounia, Drouet, Valérie, Tibar, Houyam, Souirti, Zouhayr, Ben El Haj, Rafiqua, Bouslam, Naima, Yahyaoui, Mohamed, Brice, Alexis, Benomar, Ali, Lesage, Suzanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674924/
https://www.ncbi.nlm.nih.gov/pubmed/29163333
http://dx.doi.org/10.3389/fneur.2017.00567

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674924/
https://www.ncbi.nlm.nih.gov/pubmed/29163333
http://dx.doi.org/10.3389/fneur.2017.00567

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