Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson’s disease (LARGE-PD), a case of ancestry

Mutations in Leucine Repeat Rich Kinase 2 (LRRK2), primarily located in codons G2019 and R1441, represent the most common genetic cause of Parkinson’s disease in European-derived populations. However, little is known about the frequency of these mutations in Latin American populations. In addition,...

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Detalles Bibliográficos
Autores principales: Cornejo-Olivas, Mario, Torres, Luis, Velit-Salazar, Mario R., Inca-Martinez, Miguel, Mazzetti, Pilar, Cosentino, Carlos, Micheli, Federico, Perandones, Claudia, Dieguez, Elena, Raggio, Victor, Tumas, Vitor, Borges, Vanderci, Ferraz, Henrique B., Rieder, Carlos R. M., Shumacher-Schuh, Artur, Velez-Pardo, Carlos, Jimenez-Del-Rio, Marlene, Lopera, Francisco, Chang-Castello, Jorge, Andreé-Munoz, Brennie, Waldherr, Sarah, Yearout, Dora, Zabetian, Cyrus P., Mata, Ignacio F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460260/
https://www.ncbi.nlm.nih.gov/pubmed/28649619
http://dx.doi.org/10.1038/s41531-017-0020-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460260/
https://www.ncbi.nlm.nih.gov/pubmed/28649619
http://dx.doi.org/10.1038/s41531-017-0020-6

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