Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family.

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Published in J Mol Med (Berl) on February 22, 2005

Authors

Qiufen Wang1, Mugen Liu, Chunsheng Xu, Zhaohui Tang, Yuhua Liao, Rong Du, Wei Li, Xiaoyan Wu, Xu Wang, Ping Liu, Xianqin Zhang, Jianfang Zhu, Xiang Ren, Tie Ke, Qing Wang, Junguo Yang

Author Affiliations

1: Center for Human Genome Research, Huazhong University of Science and Technology, Wuhan, Hubei, 430074, China. wangq2@ccf.org

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