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

Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease. Ten of fifteen causative genes linked to familial forms of PD have been reported to cause autosomal recessive forms. Among them, mutations in the PTEN-induced kinase 1 (PINK1) gene were...

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Detalles Bibliográficos
Autores principales:	Ben El Haj, Rafiqua, Regragui, Wafaa, Tazi-Ahnini, Rachid, Skalli, Asmae, Bouslam, Naima, Benomar, Ali, Yahyaoui, Mohamed, Bouhouche, Ahmed
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2016
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931068/ https://www.ncbi.nlm.nih.gov/pubmed/27413743 http://dx.doi.org/10.1155/2016/3460234

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