Analysis of the LRRK2 p.G2019S mutation in Colombian Parkinson's Disease Patients

INTRODUCTION: Mutations in the leucine-rich repeat kinase 2 gene (LRRK2 or Dardarin) are considered to be a common cause of autosomal dominant and sporadic Parkinson´s disease, but the prevalence of these mutations varies among populations. OBJECTIVE: to analyzed the frequency of the LRRK2 p.G2019S...

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Detalles Bibliográficos
Autores principales: Duque, Andrés Felipe, Lopez, Juan Carlos, Benitez, Bruno, Hernandez, Helena, Yunis, Juan José, Fernandez, William, Arboleda, Humberto, Arboleda, Gonzalo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Universidad del Valle 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640433/
https://www.ncbi.nlm.nih.gov/pubmed/26600626

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4640433/
https://www.ncbi.nlm.nih.gov/pubmed/26600626

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