Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only.
Wilcox R, Braenne I, Brüggemann N, Winkler S, Wiegers K, Bertram L, Anderson T, Lohmann K.
J Neurol. 2015 Jan;262(1):187-93. doi: 10.1007/s00415-014-7547-9. Epub 2014 Oct 31.