Exome sequencing identifies truncating mutations in PRRT2 that casue paroxysmal kinesigenic dyskinesia.

2011 Chen, W., Lin, Y, Xiong, Z., Wei, W, Ni, W, Tan, G., Guo, S., He, J, Chen, Y., Zhang, Q., Li, H., Lin, Y, Murong, S., Xu, J, Wang, N, Wu, Z.