Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes

Additional Metadata
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 APA Style APA-ALL Style AAA 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., Kori, I., Hattiholi, V., Jain, P., Aneja, S., Kumar, A., Gulati, P., Goel, M., Talukdar, B.& Bonifati, V. (2015). Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes. Movement Disorders, 30(7), 996–1001.https://doi.org/10.1002/mds.26202

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