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

ABSTRACT: 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...

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Autores:

Cornejo Olivas, Mario
Torres, Luis
Velit Salazar, Mario R.
Inca Martinez, Miguel
Mazzetti, Pilar
Cosentino, Carlos
Micheli, Federico
Perandones, Claudia
Dieguez, Elena
Raggio, Víctor
Tumas, Victor
Borges, Vanderci
B. Ferraz, Henrique
Rieder, Carlos R. M.
Shumacher Schuh, Artur
Vélez Pardo, Carlos
Jiménez del Río, Marlene
Lopera Restrepo, Francisco Javier
Chang Castello, Jorge
Andreé Muñoz, Brennie
Waldherr, Sarah
Yearout, Dora
Zabetian, Cyrus P.
Mata, Ignacio F.

Tipo de recurso:

Article of investigation

Fecha de publicación:

2017

Institución:

Universidad de Antioquia

Repositorio:

Repositorio UdeA

Idioma:

eng

OAI Identifier:

oai:bibliotecadigital.udea.edu.co:10495/23098

Acceso en línea:

http://hdl.handle.net/10495/23098

Palabra clave:

Rights

openAccess

License

http://creativecommons.org/licenses/by/2.5/co/