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

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