Shalash, A. S., Rösler, T. W., Müller, S. H., Salama, M., Deuschl, G., Müller, U., . . . Höglinger, G. U. (2017). c.207C>G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystonia. Neurol Genet.
Citação norma ChicagoShalash, Ali S., et al. "C.207C>G Mutation in Sepiapterin Reductase Causes Autosomal Dominant Dopa-responsive Dystonia." Neurol Genet 2017.
MLA CitationShalash, Ali S., et al. "C.207C>G Mutation in Sepiapterin Reductase Causes Autosomal Dominant Dopa-responsive Dystonia." Neurol Genet 2017.
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