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
E-mail: maganamt@gmail.com
Received: October 31, 2016; Revised: January 6, 2017; Accepted: March 30, 2017; Published online: July 1, 2017.
© The Korean Society for Laboratory Medicine. All rights reserved.

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


This Article

e-submission

Archives

Indexed/Covered by