Dystonia, Genetics, Manganese, Metabolic inherited disease, SLC30A10
dx.doi.org/10.1002/mds.26202, hdl.handle.net/1765/88424
Movement Disorders
Erasmus MC: University Medical Center Rotterdam

Quadri, M, Kamate, M, Sharma, S, Olgiati, S, Graafland, J, Breedveld, G.J, … Bonifati, V. (2015). Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes. Movement Disorders, 30(7), 996–1001. doi:10.1002/mds.26202