Article info
PDFGenotype-phenotype correlations
Original research
Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients
- Correspondence to Dr Hui Xiong, Department of Pediatrics, Peking University First Hospital, Beijing 100034, China; xh_bjbj{at}163.com; Dr Hong Zhang, Institute of Cardiovascular Sciences and Key Laboratory of Molecular Cardiovascular Sciences, Peking University Health Science Center, Beijing, China; zhanghong{at}bjmu.edu.cn
Citation
Clinical spectrum and genetic variations of LMNA-related muscular dystrophies in a large cohort of Chinese patients
Publication history
- Received November 1, 2019
- Revised April 11, 2020
- Accepted May 2, 2020
- First published June 22, 2020.
Online issue publication
April 27, 2021
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© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.