A recurrent mutation in KCNA2 as a novel cause of hereditary spastic paraplegia and ataxia
Authors: 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
Collaborators: Children's Hospital of Philadelphia; German Center for Neurodegenerative Diseases; Linköping University; Oulu University Hospital; University Medical Center Schleswig-Holstein, Christian-Albrechts-University; University of Helsinki; University of Leipzig Hospitals and Clinics; University of Tübingen; University of Utah