Replacement therapy in the mucopolysaccharidoses

Author:

Dean M. F.

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference40 articles.

1. The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase;Bach, G.; Eisenberg, Jr., F.; Cantz, M.; Neufeld, E.F.;Proceedings ofthe National Academy of Sciences of the United States of America,1973

2. The defect in Hurler and Scheie Syndromes: Deficiency of a-L-iduronidase;Bach, G.; Friedman, R.; Weissmann, B.; Neufeld, E.F.;Proceedings of the National Academy of Sciences of the United States of America,1972

3. In-vitro correction of deficient human fibroblasts by P-glucuronidase from different human sources;Brot, F.E.; Glaser, J.H.; Roozen, K.J.; Sly, W.S.; Stahl, P.D.;Biochemical and Biophysical Researcht Communications,1974

4. The Hunter corrective factor: purification and preliminary characterisation;Cantz, M.; Chrambach, A.; Bach, G.; Neufeld, E.F.;Journal of Biological Chemistry,1972

5. Dean, M. F., Benson, P. F., and Muir, H. (1973).

Cited by 3 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. MORPHOLOGICAL AND BIOCHEMICAL ANALYSIS OF BIOPSY SPECIMENS IN DISORDERS OF SKELETAL DEVELOPMENT;Acta Paediatrica;1982-05

2. The muscle cell;Journal of Clinical Pathology;1978-01-01

3. Diseases of connective tissue: a consensus;Journal of Clinical Pathology;1978-01-01

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