Author:
Roth J.,Schulze E.,Raabe G.,Waldmann G.
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology,General Medicine,Pathology and Forensic Medicine,Histology,Pathology and Forensic Medicine,Anatomy
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3. Beutler, E., Kuhl, W.: Biochemical and electrophoretio studies of ?-galactosidase in normal man, in patients with Fabry's disease, and in Equidae. Amer. J. hum. Genet. 24, 237?249 (1972)
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5. Brady, R. D., Tallmann, J. F., Johnson, W. G., Gal, A. E., Leaky, W. R., Quirk, J. M., Dekaban, A. S.: Replacement therapy for inherited enzyme deficiency. Use of purified Ceramidtrihexosidase in Fabry's disease. New Engl. J. Med. 289, 9?14 (1973)
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