Gene, Cell and Tissue

Published by: Kowsar

A Novel Deletion Mutation of the TYR Gene in a Patient With Oculocutaneous Albinism Type 1A

Farah Talebi 1 , Farideh Ghanbari 2 , * and Javad Mohammadi Asl 3
Authors Information
1 Milad Genetic Counseling Center, Ahvaz, IR Iran
2 Department of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, IR Iran
3 Department of Medical Genetics, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran
Article information
  • Gene, Cell and Tissue: January 01, 2016, 3 (1); e33678
  • Published Online: January 16, 2016
  • Article Type: Case Report
  • Received: October 7, 2015
  • Revised: November 10, 2015
  • Accepted: November 24, 2015
  • DOI: 10.17795/gct-33678

To Cite: Talebi F, Ghanbari F, Mohammadi Asl J. A Novel Deletion Mutation of the TYR Gene in a Patient With Oculocutaneous Albinism Type 1A, Gene Cell Tissue. 2016 ; 3(1):e33678. doi: 10.17795/gct-33678.

Abstract
Copyright © 2016, Zahedan University of Medical Sciences. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
1. Introduction
2. Case Presentation
3. Discussion
References
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