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For contributors- Clinical and molecular characterization of Korean children with infantile and late-onset Pompe disease: 10 years of experience with enzyme replacement therapy at a single center
- Min-Sun Kim, Ari Song, Minji Im et al.
- Clin Exp Pediatr. 2019;62(6):224-234.
- A study of the relationship between clinical phenotypes and plasma iduronate-2-sulfatase enzyme activities in Hunter syndrome patients
- Ok Jeong Lee, Su-Jin Kim, Young Bae Sohn et al.
- Clin Exp Pediatr. 2012;55(3):88-92.