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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| Udgivet i: | Colombia Médica |
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| Principais autores: | , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Universidad del Valle
2015
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| Fag: | |
| Online adgang: | 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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