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Autor:
Yo-Kyung Chung, Chihwa Kim, Eui-cheol Jo, Jinwook Seo, Jongmun Sohn, Byoung-Ju Lee, Hyi-Jeong Ji, Jaehyeon Lee
Publikováno v:
Journal of Human Genetics
Hunter syndrome is an X-linked lysosomal storage disease caused by a deficiency in the enzyme iduronate-2-sulfatase (IDS), leading to the accumulation of glycosaminoglycans (GAGs). Two recombinant enzymes, idursulfase and idursulfase beta are current
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::263f8755ed3aa2eec25773590acb6418
https://pubmed.ncbi.nlm.nih.gov/27829684
https://pubmed.ncbi.nlm.nih.gov/27829684
