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

ABSTARCT: Mutations in Leucine-Rich Repeat 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...

Full description

Autores:

Cornejo Olivas, Mario Reynaldo
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 Ballalai
de Mello Rieder, Carlos Roberto
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

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:10495/11959

Acceso en línea:

http://hdl.handle.net/10495/11959

Palabra clave:

Genetics of Parkinson's disease
LRRK2
LARGE-PD
Parkinson Disease
Enfermedad de Parkinson

Rights

openAccess

License

Atribución 2.5