Ann Lab Med 2017; 37(4): 355-358
Homozygous LPL p.Gly188Glu Mutation in a Mexican Girl With Lipoprotein Lipase Deficiency
Ana Gabriela Colima Fausto, M.S.1,2, Juan Ramón González García, Ph.D.1, Teresita De Jesús Hernández Flores, B.S.1,2, Norma Alejandra Vázquez Cárdenas, Ph.D.3, Nery Eduardo Solís Perales, M.D.4, and María Teresa Magaña Torres, Ph.D.1,2
Genetic Division1, Western Biomedical Research Center, Mexican Institute of Social Security, Guadalajara, Jalisco; Doctorate Program in Human Genetics2, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco; Autonomous University of Guadalajara3, Guadalajara; Pediatric Hospital of the Public Health Institute of the State of Guanajuato4, Guanajuato, Mexico
Correspondence to: María Teresa Magaña Torres
Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social. Sierra Mojada No. 800. Col. Independencia. Guadalajara, Jal. C.P. 44340, México
Tel: +52-33-36-17-00-60 ext. 31929, 31930
Received: October 31, 2016; Revised: January 6, 2017; Accepted: March 30, 2017; Published online: July 1, 2017.
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