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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, Hyung-Doo Park, Soo-Youn Lee, Chi-Hwa Kim, Ah-Ra Ko, Yeon-Joo Yook, Su-Jin Lee, Sung Won Park, Se-Hwa Kim, Sung-Yoon Cho, Eun-Kyung Kwon, Sun Ju Han, Dong-Kyu Jin
Clin Exp Pediatr. 2012;55(3):88-92.   Published online March 16, 2012
DOI: https://doi.org/10.3345/kjp.2012.55.3.88

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A study of the relationship between clinical phenotypes and plasma iduronate-2-sulfatase enzyme activities in Hunter syndrome patients
Korean Journal of Pediatrics. 2012;55(3):88   Crossref logo
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Idursulfase enzyme replacement therapy in an adult patient with severe Hunter syndrome having a novel mutation of iduronate-2-sulfatase gene
Clinica Chimica Acta. 2013;423:66-68   Crossref logo
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Administration of iduronate sulfatase by plasma exchange to patients with the hunter syndrome: A clinical study
American Journal of Medical Genetics. 1982;13(3):309-318   Crossref logo
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Assessment of iduronate-2-sulfatase mRNA expression in Hunter syndrome (mucopolysaccharidosis type II)
Human Genetics. 1992;90(3):   Crossref logo
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Diagnosis of Hunter syndrome: identification of iduronate-2-sulfatase gene mutations in patients with mucopolysaccharidosis type II in Chinese
Fertility and Sterility. 2003;80:290   Crossref logo
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Mutations of the iduronate-2-sulfatase gene on a T146T background in three patients with Hunter syndrome
Human Mutation. 1995;5(3):272-274   Crossref logo
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Mutations of the iduronate-2-sulfatase (IDS) gene in patients with hunter syndrome (mucopolysaccharidosis II)
Human Mutation. 1994;4(2):128-131   Crossref logo
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Hunter syndrome: presence of material cross-reacting with antibodies against iduronate sulfatase
Human Genetics. 1987;75(3):234-238   Crossref logo
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A deletion involving exons 2-4 in the iduronate-2-sulfatase gene of a patient with intermediate Hunter syndrome
Clinical Genetics. 2008;53(6):474-477   Crossref logo
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Identification of iduronate sulfatase gene alterations in 70 unrelated Hunter patients
Clinical Genetics. 2008;53(5):362-368   Crossref logo
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