Iranian Journal of Pediatrics

Published by: Kowsar

Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene

Mahin Hashemipour 1 , Mehdi Khorrami 2 , Manijeh Mahdavi 2 , Maryam Hosseindokht Khujin 2 and Majid Kheirollahi 2 , *
Authors Information
1 Endocrine and Metabolism Research Center, Isfahan University of Medical Sciences, Isfahan, IR Iran
2 Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-communicable Disease AND Genetics and Molecular Biology Department, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IR Iran
Article information
  • Iranian Journal of Pediatrics: February 2018, 28 (1); e6921
  • Published Online: February 18, 2018
  • Article Type: Research Article
  • Received: May 8, 2016
  • Revised: November 22, 2017
  • Accepted: January 18, 2018
  • DOI: 10.5812/ijp.6921

To Cite: Hashemipour M, Khorrami M, Mahdavi M, Hosseindokht Khujin M, Kheirollahi M. et al. Allgrove Syndrome in Iranian Patients and Report on a Novel Mutation in AAAS Gene, Iran J Pediatr. 2018 ;28(1):e6921. doi: 10.5812/ijp.6921.

Abstract
Copyright: Copyright © 2018, Iranian Journal of Pediatrics. 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. Methods
3. Results
4. Discussion
Acknowledgements
References
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