Newborn screening for six lysosomal storage disorders in a cohort of Mexican patients: Three-year findings from a screening program in a closed Mexican health system.

Autor: Navarrete-Martínez JI; Department of Genetics, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico., Limón-Rojas AE; General Dictatorate, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico., Gaytán-García MJ; Department of Genetics, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico., Reyna-Figueroa J; Department of Medical Education and Research, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico., Wakida-Kusunoki G; General Dictatorate, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico., Delgado-Calvillo MDR; Department of Pediatrics, Hospital Regional de Villahermosa, PEMEX, Villahermosa, Tabasco, Mexico., Cantú-Reyna C; Genomi-k SAPI de CV. Monterrey, Nuevo León, Mexico; Escuela de Medicina Tecnológico de Monterrey, Monterrey, Nuevo León, Mexico., Cruz-Camino H; Genomi-k SAPI de CV. Monterrey, Nuevo León, Mexico; Escuela de Biotecnología y Ciencias de la Salud, Tecnológico de Monterrey, Monterrey, Nuevo León, Mexico., Cervantes-Barragán DE; Department of Genetics, Hospital Central Sur de Alta Especialidad, PEMEX, Mexico City, Mexico; Facultad Mexicana de Medicina, Universidad La Salle, Mexico City, Mexico. Electronic address: david.eduardo.cervantes@pemex.com.

Publikováno v: Molecular genetics and metabolism [Mol Genet Metab] 2017 May; Vol. 121 (1), pp. 16-21. Date of Electronic Publication: 2017 Mar 09.