Multiple Sulfatase Deficiencies in Cultured Skin Fibroblasts
Author:
Publisher
American Medical Association (AMA)
Subject
Clinical Neurology,Arts and Humanities (miscellaneous)
Cited by 67 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Multiple Sulfatase Deficiency: A Disease Comprising Mucopolysaccharidosis, Sphingolipidosis, and More Caused by a Defect in Posttranslational Modification;International Journal of Molecular Sciences;2020-05-13
2. Multiple sulfatase deficiency;Atlas of Inherited Metabolic Diseases 3E;2011-12-30
3. Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann–Pick C1 disease — Lysosomal storage disorders caused by defects of non-lysosomal proteins;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2009-04
4. Hunter disease (mucopolysaccharidosis type II) in a karyotypically normal girl;Clinical Genetics;2008-06-28
5. Long-term follow-up of a girl with Maroteaux-Lamy syndrome after bone marrow transplantation;World Journal of Pediatrics;2008-05
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