Author:
Cooper A.,Hatton C.,Thornley M.,Sardharwalla I. B.
Subject
Genetics (clinical),Genetics
Reference35 articles.
1. Baum, H., Dodgson, K. S. and Spencer, B. The assay of aryl sulphatases A and B in human urine.Clin. Chim. Acta 4 (1959) 453–455
2. Beaudet, A. L. Disorders of glycoprotein degradation: mannosidosis, fucosidosis, sialidosis and aspartylglycosaminuria. In Stanbury, J. W., Wyngaarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S. (eds.),The Metabolic Basis of Inherited Disease, McGraw-Hill, New York, 1983, pp. 788–802
3. Besley, G. T. N. and Gat, S. Spectrophotometric and fluorimetric assays of galactocerebrosidase activity, their use in the diagnosis of Krabbe's disease.Clin. Chim. Acta 110 (1981) 19–26
4. Cooper, A., Hatton, C. and Sardharwalla, I. B. Acid β-mannosidase of human plasma: influence of age and sex on enzyme activity.J. Inher. Metab. Dis. 10 (1987) In press.
5. Cooper, A., Sardharwalla, I. B. and Roberts, M. M. Human β-mannosidase deficiency.N. Engl. J. Med. 315 (1986) 1231
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