Cite
Enzyme replacement therapy in two patients with an advanced severe (Hurler) phenotype of mucopolysaccharidosis I.
MLA
Tokic, Visnja, et al. “Enzyme Replacement Therapy in Two Patients with an Advanced Severe (Hurler) Phenotype of Mucopolysaccharidosis I.” European Journal of Pediatrics, vol. 166, no. 7, July 2007, pp. 727–32. EBSCOhost, https://doi.org/10.1007/s00431-006-0316-8.
APA
Tokic, V., Barisic, I., Huzjak, N., Petkovic, G., Fumic, K., & Paschke, E. (2007). Enzyme replacement therapy in two patients with an advanced severe (Hurler) phenotype of mucopolysaccharidosis I. European Journal of Pediatrics, 166(7), 727–732. https://doi.org/10.1007/s00431-006-0316-8
Chicago
Tokic, Visnja, Ingeborg Barisic, Nevenka Huzjak, Giorgie Petkovic, Ksenija Fumic, and Eduard Paschke. 2007. “Enzyme Replacement Therapy in Two Patients with an Advanced Severe (Hurler) Phenotype of Mucopolysaccharidosis I.” European Journal of Pediatrics 166 (7): 727–32. doi:10.1007/s00431-006-0316-8.