Bally, J. F., Breen, D. P., Schaake, S., Trinh, J., Rakovic, A., Klein, C., & Lang, A. E. (2020). Mild dopa-responsive dystonia in heterozygous tyrosine hydroxylase mutation carrier: Evidence of symptomatic enzyme deficiency? Parkinsonism Relat Disord.
Chicago Stili AlıntıBally, Julien F., David P. Breen, Susen Schaake, Joanne Trinh, Aleksandar Rakovic, Christine Klein, ve Anthony E. Lang. "Mild Dopa-responsive Dystonia in Heterozygous Tyrosine Hydroxylase Mutation Carrier: Evidence of Symptomatic Enzyme Deficiency?" Parkinsonism Relat Disord 2020.
MLA AlıntıBally, Julien F., et al. "Mild Dopa-responsive Dystonia in Heterozygous Tyrosine Hydroxylase Mutation Carrier: Evidence of Symptomatic Enzyme Deficiency?" Parkinsonism Relat Disord 2020.