Mostrando 3 resultados de: 3
Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients
ArticleAbstract: Background: Parkinson's disease is the second most common neurodegenerative disorder and affects peoPalabras claves:copy number variants, Genetics, Latin America, Parkinson's DiseaseAutores:Acosta G.T., Amorin I., Arboleda G., Arboleda H., Arboleda-Bustos C.E., Borges V., Chana-Cuevas P., Cornejo-Olivas M., Cosentino C., Dieguez E., Fernandez W., Ferraz H.B., Ferrera A., Fornaguera J., Gatto E.M., Guillén A.H., Horimoto A.V.R., Inca-Martinez M., Jimenez-Del-Rio M., Jorge Chang-Castello, Lal D., Lescano A.G., Loesch D., Lopera F., Martinez-Ramirez D., Mata I.F., Mazzetti P., Medina A., Micheli F., Moreno S., Muñoz B.A., Niestroj L.M., Orozco J.L., O´Connor T.D., Pérez-Palma E., Raggio V., Rieder C.R.M., Rivera A., Rivera-Valdivia A., Rodriguez M., Santos-Lobato B.L., Sarapura H., Sarapura-Castro E., Sarihan E.I., Shumacher-Schuh A., Thornton T.A., Torres L., Tumas V., Velez-Pardo C., Viñuela A., Yearout D., Zabetian C.P.Fuentes:scopusErratum: Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson’s disease (LARGE-PD), a case of ancestry (npj Parkinson's Disease, (2017), 3, 1, (19), 10.1038/s41531-017-0020-6)
OtherAbstract: The original version of this article contained an error in the name of gene LRRK2, which was incorrePalabras claves:Autores:Andree-Muñoz B., Borges V., Cornejo-Olivas M., Cosentino C., Dieguez E., Ferraz H.B., Inca-Martinez M., Jimenez-Del-Rio M., Jorge Chang-Castello, Lopera F., Mata I.F., Mazzetti P., Micheli F., Perandones C., Raggio V., Rieder C.R.M., Shumacher-Schuh A., Torres L., Tumas V., Velez-Pardo C., Velit-Salazar M.R., Waldherr S., Yearout D., Zabetian C.P.Fuentes:scopusVariable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry /692/617/375/1718 /631/208/1516 article
ArticleAbstract: Genetic risk: Uncovering ethnic-specific mutations: A new study reveals the frequency of Leucine RepPalabras claves:Autores:Andree-Muñoz B., Borges V., Cornejo-Olivas M., Cosentino C., Dieguez E., Ferraz H.B., Inca-Martinez M., Jimenez-Del-Rio M., Jorge Chang-Castello, Lopera F., Mata I.F., Mazzetti P., Micheli F., Perandones C., Raggio V., Rieder C.R.M., Shumacher-Schuh A., Torres L., Tumas V., Velez-Pardo C., Velit-Salazar M.R., Waldherr S., Yearout D., Zabetian C.P.Fuentes:scopus