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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Publié dans:	Colombia Médica
Auteurs principaux:	Andrés Felipe Duque, Juan Carlos Lopez, Bruno Benitez, Helena Hernandez, Juan José Yunis, William Fernandez, Humberto Arboleda, Gonzalo Arboleda
Format:	Artigo
Langue:	Inglês
Publié:	Universidad del Valle 2015
Sujets:	Medicina
Accès en ligne:	https://www.redalyc.org/articulo.oa?id=28342288005 https://www.redalyc.org/journal/283/28342288005/ https://www.redalyc.org/journal/283/28342288005/html/ https://www.redalyc.org/journal/283/28342288005/28342288005.epub https://www.redalyc.org/journal/283/28342288005/movil
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