Enzyme replacement therapy in two patients with an advanced severe (Hurler) phenotype of mucopolysaccharidosis I - Concepedia

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Enzyme replacement therapy in two patients with an advanced severe (Hurler) phenotype of mucopolysaccharidosis I

45

Citations

7

References

2006

Year

Višnja Tokić, Ingeborg Barišić, Nevenka Huzjak, Giorgie Petković, Ksenija Fumić, Eduard Paschke

European Journal of Pediatrics

Advanced SevereEnzyme Replacement TherapyPathologyMedicineLysosomal Storage Disease

References

	Year	Citations

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