Clinical Significance of Enzyme Deficiencies

Beutler E. (1966). Glucose-6-phosphate dehydrogenase deficiency. Chapter 47 in Stanbury J. B. Wyngaarden J. B. Frederickson D. S. (1966) The metabolic basis of inherited disease, 2nd edition. London: McGraw-Hill.

Dixon M. Webb E. C. (1964). Enzymes, Edition 2, p. 5. London: Longmans.

Froesch E. R. (1966). Essential fructosuria and hereditary fructose intolerance. Chapter 6 in Stanbury J. B. Wyngaarden J. B. Frederickson D. S. (1966) The metabolic basis of inherited disease, 2nd edition. London: McGraw-Hill.

Harris H. (1961). Congenital abnormalities of enzyme formation, p. 92. In Proc. of 4th Int. Congress of clinical chemistry. London: Butterworth.

Holt L. E. Jr. Snyderman S. E. (1964). Anomalies of amino-acid metabolism in mammalian protein metabolism, ch. 18. Edited by Munro H. N. Allison J. B. London: Acad. Press.

Hutchison J. H. (1964). Practical paediatric problems, p. 316. London: Lloyd-Luke.

McGirr E. M. (1963). In The thyroid and its diseases, p. 52. Edited by Mason A. S. London: Pitman Medical.

Stanbury J.B. Wyngaarden J. B. Frederickson D. S. (1966). The Metabolic basis of inherited disease, 2nd edition. London: McGraw-Hill.

Wilkinson J. H. (1962). An introduction to diagnostic enzymology. London: Arnold.

Woolf L. I. (1962). Galactosemia. In Advances in clinical chemistry, vol. 5. Edited by Sobotka H. Stewart C. P. London: Acad. Press.

Woolf L. I. (1963). Phenylketonuria. In Clinical chemistry, Vol. 6. Edited by Sobotka H. Stewart C. P. London: Acad. Press.