Cataract and metabolic disease

Author:

Endres W.,Shin Y. S.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference53 articles.

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2. Beaudet, A. L. and Thomas, G. H. Disorders of glycoprotein degradation: mannosidosis, fucosidosis, sialidosis, and aspartylglycosaminuria. In Scriver, C. R., Beaudet, A. L., Sly, W. S. and Valle, D. (eds.),The Metabolic Basis of Inherited Disease, McGraw-Hill, New York, 1989, pp. 1603–1621

3. Beutler, E. and Matsumoto, F. Galactokinase and cataracts.Lancet 1 (1978) 1161

4. Beutler, E., Matsumoto, F., Kuhl, W., Krill, A., Levy, N., Sparkes, R. and Degnan, M. Galactokinase deficiency as a cause of cataracts.N. Engl. J. Med. 228 (1973) 1203–1206

5. Björkhem, I. and Skrede, S. Familial diseases with storage of sterols other than cholesterol: Cerebrotendinous xanthomatosis and phytosterolemia. In Scriver, C. R., Beaudet, A. L., Sly, W. S. and Valle, D. (eds.),The Metabolic Basis of Inherited Disease, McGraw-Hill, New York, 1989, pp. 1283–1302

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