Enzymes

Author:

Saifer Abraham

Publisher

Springer US

Reference166 articles.

1. Stoffel, W., Sphingolipids, Annu. Rev. Biochem. 40: 57 (1971).

2. Fredrickson, D. S. and Sloan, H. R., Glucosylceramide lipidoses. Gaucher’s disease, in: The Metabolic Basis of Inherited Disease, J. B. Stanbury, J. B. Wyngaarden, and D. S. Fredrickson, eds., McGraw-Hill, New York, 3rd ed., pp. 730–759 (1972).

3. Sweeley, C. C., Klionsky, B., Krivit, W., and Desnick, R. J., Fabry’s disease. Glycosphingolipid lipidosis, in: The Metabolic Basis of Inherited Disease, J. B. Stanbury, J. B. Wyngaarden, and D. S. Fredrickson, eds., McGraw-Hill, New York, 3rd ed., pp. 663–687 (1972).

4. Suzuki, K. and Suzuki, Y., Galactosyl ceramide lipidosis: Globoid cell leucodystrophy (Krabbe’s disease), in: The Metabolic Basis of Inherited Disease, J. B. Stanbury, J. B. Wyngaarden, and D. S. Fredrickson, eds., McGraw-Hill, New York, 3rd ed., pp. 760–782 (1972).

5. Dawson, G., Matalon, R., and Stein, A. O., Lactosylceramidosis: Lactosylceramide galactosyl hydrolase deficiency and accumulation of lactosylceramide in cultured skin fibroblasts, J. Pediatr. 79: 423 (1971).

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