A missense mutation in the KCTD17 gene causes autosomal dominant myoclonus-dystonia
Year: 2015
Type: conference-paper
Authors: Mencacci, NE, Rubio-Augusti, I, Zdebik, A, Asmus, F, Ludtmann, M, Hauser, AK, Plagnol, V, Pittman, A, Bandres-Ciga, S, Soutar, M, Peall, K, Morris, H, Trabzuni, D, Ryten, M, Tekman, M, Stanescu, H, Kleta, R, Carecchio, M, Nardocci, N, Garavaglia, B, Lohmann, E, Weissbach, A, Klein, C, Hardy, J, Abramov, AY, Foltynie, T, Gasser, T, Bhatia, KP, Wood, NW
Language: English
Subfield: Clinical Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2885380475