- Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family. Wang, Q., Liu, M., Xu, C., Tang, Z., Liao, Y., Du, R., Li, W., Wu, X., Wang, X., Liu, P., Zhang, X., Zhu, J., Ren, X., Ke, T., Wang, Q., Yang, J. J. Mol. Med. (2005)