De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient

Klein, C., Baumann, H., Olschewski, L., Hanssen, H., Münchau, A., Ferbert, A., … Lohmann, K. (2019, July 1). De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient. Parkinsonism and Related Disorders. Elsevier Ltd. https://doi.org/10.1016/j.parkreldis.2019.03.018