Article info
PostScript
Letter
Whole-exome sequencing identified novel KIF5A mutations in Chinese patients with amyotrophic lateral sclerosis and Charcot-Marie-Tooth type 2
- Correspondence to Professor Dongsheng Fan, Neurology, Peking University Third Hospital, Beijing 100191, China; dsfan2010{at}aliyun.com
Citation
Whole-exome sequencing identified novel KIF5A mutations in Chinese patients with amyotrophic lateral sclerosis and Charcot-Marie-Tooth type 2
Publication history
- Received January 26, 2019
- Revised July 16, 2019
- Accepted July 31, 2019
- First published August 17, 2019.
Online issue publication
February 13, 2020
Article Versions
- Previous version (17 August 2019).
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© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.