doi.org/10.1002/mds.25390, hdl.handle.net/1765/53935
Movement Disorders
Department of Clinical Genetics

Delnooz, C., Wevers, R., Quadri, M., Clayton, P., Mills, P., Tuschl, K., … van de Warrenburg, B. (2013). Phenotypic variability in a dystonia family with mutations in the manganese transporter gene. Movement Disorders, 28(5), 685–686. doi:10.1002/mds.25390