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A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia
- Correspondence to Dr H Y Edwin Chan, School of Life Sciences, Room 509B, Mong Man Wai Building, The Chinese University of Hong Kong, Hong Kong, Hong Kong; hyechan{at}cuhk.edu.hk Dr Ting-Fung Chan, School of Life Sciences, Room 177, Science Centre South Block, The Chinese University of Hong Kong, Hong Kong; tf.chan@cuhk.edu.hk
Citation
A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia
Publication history
- Received February 10, 2014
- Revised June 9, 2014
- Accepted July 5, 2014
- First published July 25, 2014.
Online issue publication
April 27, 2016
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Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) 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 and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/