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Enzyme replacement in Pompe disease: An attempt with purified human α-glucosidase
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de Barsy, T., Jacquemin, P., Van Hoof, F., and Hers, H. G. (1973). Enzyme replacement in Pompe disease: an attempt with purified human α-glucosidase. Enzyme Therapy and Genetic Diseases, Birth Defects, Original Article Series, 9:184-190.
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The lysosome concept
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Lejeune, N., Thinès-Sempoux, D., and Hers, H. G. (1963). Tissue fractionation studies. 16. Intracellular distribution and properties of α-glucosidases in rat liver. Biochem. J. 86:16-21.
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The abnormalities of lysosomal enzymes in mucopolysacccharidoses
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Van Hoof, F. and Hers, H. G. (1968). The abnormalities of lysosomal enzymes in mucopolysacccharidoses. Eur. J. Biochem. 7:34-44.
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Reuck, A. V. S. and Cameron, M. P. Eds., London: J. & A. Churchill
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Wattiaux, R., Wibo, M., and Baudhuin, P. (1963). Influence of the injection of Triton WR-1339 on the properties of rat-liver lysosomes. In: Reuck, A. V. S. and Cameron, M. P. (Eds.), Ciba Foundation Symposium on Lysosomes, London: J. & A. Churchill, pp. 176-200.
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