![A recurrent mutation in
<i>KCNA2</i>
as a novel cause of hereditary spastic paraplegia and ataxia]()
A recurrent mutation in
<i>KCNA2</i>
as a novel cause of hereditary spastic paraplegia and ataxiaHelbig, Katherine L.; Hedrich, Ulrike B. S.; Shinde, Deepali N.; Krey, Ilona; Teichmann, Anne-Christin; Hentschel, Julia; Schubert, Julian; Chamberlin, Adam C.; Huether, Robert; Lu, Hsiao-Mei; Alcaraz, Wendy A.; Tang, Sha; Jungbluth, Chelsy; Dugan, Sarah L.; Vainionpää, Leena; Karle, Kathrin N.; Synofzik, Matthis; Schöls, Ludger; Schüle, Rebecca; Lehesjoki, Anna-Elina; Helbig, Ingo; Lerche, Holger; Lemke, Johannes R. · Annals of Neurology · 2016