In observance of Labor Day, Ambry’s business office will be closed on Monday, September 7th, 2026. While our lab will remain open to run in-progress tests, we will not receive sample deliveries from FedEx®️.
Close top bar

Back to Publications

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

Specialty Areas:
Date: June 1, 2023
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
Journal: Annals of neurology
Journal Volume: 80
Topics:
Collaborators:
Read Abstract