Iranian Journal of Pediatrics

Published by: Kowsar

Novel Gene LAMA2 Mutation and Exonic Deletion Underline Merosin-Deficient Congenital Muscular Dystrophy 1A in a Chinese Family

Lili Liang 1 , Qigang Zhang 1 and Xuefan Gu 1 , *
Authors Information
1 Department of Pediatric Endocrinology and Genetics, Shanghai Institute for Pediatric Research, Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China
Article information
  • Iranian Journal of Pediatrics: April 2017, 27 (2); e1884
  • Published Online: February 4, 2017
  • Article Type: Case Report
  • Received: April 8, 2015
  • Revised: October 3, 2016
  • Accepted: January 21, 2017
  • DOI: 10.5812/ijp.1884

To Cite: Liang L, Zhang Q, Gu X. Novel Gene LAMA2 Mutation and Exonic Deletion Underline Merosin-Deficient Congenital Muscular Dystrophy 1A in a Chinese Family, Iran J Pediatr. 2017 ; 27(2):e1884. doi: 10.5812/ijp.1884.

Abstract
Copyright © 2017, Growth & Development Research Center. 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
Acknowledgements
References
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