A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia

Katherine L. Helbig, Ulrike B. S. Hedrich, Deepali N. Shinde, Ilona Krey, Anne-Christin Teichmann, Julia Hentschel, Julian Schubert, Adam C. Chamberlin, Robert Huether, Hsiao-Mei Lu, Wendy A. Alcaraz, Sha Tang, Chelsy Jungbluth, Sarah Dugan, Leena Vainionpaa, Kathrin Karle, Matthis Synofzik, Ludger Schöls, Rebecca Schüle, Anna-Elina Lehesjoki, Ingo Helbig, Holger Lerche, Johannes R. Lemke