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Erratum: 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