Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes

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Keywords	Dystonia, Genetics, Manganese, Metabolic inherited disease, SLC30A10
Persistent URL	doi.org/10.1002/mds.26202, hdl.handle.net/1765/88424
Journal	Movement Disorders
Organisation	Erasmus MC: University Medical Center Rotterdam
Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style American-Institute-of-Physics Style Council-of-Science-Editors Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format	Quadri, M., Kamate, M., Sharma, S., Olgiati, S., Graafland, J., Breedveld, G., … Bonifati, V. (2015). Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes. Movement Disorders, 30(7), 996–1001. doi:10.1002/mds.26202

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