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BMJ Publishing Group, Journal of Medical Genetics, 9(51), p. 590-595, 2014

DOI: 10.1136/jmedgenet-2014-102333

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A novel missense mutation inCCDC88Cactivates the JNK pathway and causes a dominant form of spinocerebellar ataxia

Journal article published in 2014 by Ho Tsoi, Allen C. S. Yu, Zhefan S. Chen, Nelson K. N. Ng, Anne Y. Y. Chan, Liz Y. P. Yuen, Jill M. Abrigo, Suk Ying Tsang, Stephen K. W. Tsui, Tony M. F. Tong, Ivan F. M. Lo, Stephen T. S. Lam, Vincent C. T. Mok, Lawrence K. S. Wong, Jacky C. K. Ngo and other authors.
This paper is available in a repository.
This paper is available in a repository.

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