A recurrent mutation in KCNA2 in complicated autosomal dominant spastic paraplegia: An expansion of the channelopathy spectrum and a novel disease mechanism

K.L. Helbig, U.B.S. Hedrich, A.C. Teichmann, J. Hentschel, D.N. Shinde, W.A. Alcaraz, S. Tang, C. Jungbluth, S.L. Dugan, R. Schu00fcle, H. Lerche, J.R. Lemke