About this Journal Submit a Manuscript Table of Contents
BioMed Research International
Volume 2013 (2013), Article ID 342371, 6 pages
http://dx.doi.org/10.1155/2013/342371
Research Article

UGT1A1 Gene Mutation due to Crigler-Najjar Syndrome in Iranian Patients: Identification of a Novel Mutation

1Department of Medical Genetics, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
2Genetic Department, Faculty of Science, Shahid Chamran Univerity, Ahvaz, Iran
3Pediatric Department, Ahvaz Jundishapur University of Medical Sciences, Golestan Hospital, Golestan, Ahvaz, Iran
4Noor Genetic Diagnostic Laboratory, Ahvaz, Iran
5Toxicology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran

Received 9 April 2013; Revised 27 June 2013; Accepted 27 June 2013

Academic Editor: Thomas Liehr

Copyright © 2013 Javad Mohammadi Asl et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Javad Mohammadi Asl, Mohammad Amin Tabatabaiefar, Hamid Galehdari, et al., “UGT1A1 Gene Mutation due to Crigler-Najjar Syndrome in Iranian Patients: Identification of a Novel Mutation,” BioMed Research International, vol. 2013, Article ID 342371, 6 pages, 2013. doi:10.1155/2013/342371