Author:
van der Ploeg A. T.,Loonen M. C. B.,Bolhuis P. A.,Reuser A. J. J.
Reference33 articles.
1. J.C. Fratantoni, C.W. Hall, and E.F. Neufeld, Hurler and Hunter syndromes: Mutual correction of the defect in cultured fibroblasts, Science 162:570 (1968).
2. P. Baudhuin, H.G. Hers, and H. Loeb, An electron microscopic and biochemical study of type II Glycogenosis, Lab. Invest. 13:1139 (1964).
3. G. Hug, and W.K. Schubert, Lysosomes in type II Glycogenosis. Changes during administration of extract from Aspergillus Niger, Cell. Biol. 35:C1 (1967).
4. R.O. Brady, J.F. Tallman, W.G. Johnson, A.E. Gal, W.R. Leahy, J.M. Quirk, and A.S. Dekaban, Replacement therapy for inherited enzyme deficiency. Use of purified ceramidetrihexosidase in Fabry’s disease, New. Engl. J. Med. 289:9 (1973).
5. R.J. Desnick, ed., Enzyme therapy in genetic diseases: 2, Alan R. Liss, New York (1980).