1. Kredich, N. M. and Hershfield, M. S. (1983) Immunodeficiency diseases caused by adenosine deaminase deficiency and purine nucleoside phosphorylase deficiency. In:The Metabolic Basis of Inherited Disease, Chapter 43 (Stanbury, J. B., Wyngaarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S., eds.) Plenum Press, NY, pp. 1157?1183.
2. Morgan, G., Levinsky, R. J., Hugh-Jones, K., Fairbanks, L. D., Morris, G. S. and Simmonds, H. A. (1987) Heterogeneity of biochemical, clinical and immunological parameters in severe combined immunodeficiency due to adenosine deaminase deficiency.Clin. exp. Immunol. 70:491?499.
3. Simmonds, H. A., Panayi, G. S. and Corrigal, V. (1978) A role for purine metabolism in the immune response: adenosine deaminase activity and deoxyadenosine catabolism.Lancet 1:60?63.
4. Hershfield, M. S. (1979) Apparent suicide inactivation of human lymphoblast S-adenosylhomocysteine hydrolase by 2?-deoxyadenosine and adenine arabinoside. A basis for direct toxic effects of analogs of adenosine.J. Biol. Chem. 254:22?25.
5. Fairbanks, L. D., Simmonds, H. A. and Webster D. R. (1987) Use of intact erythrocytes in the diagnosis of inherited purine and pyrimidine disorders.J. Inher. Metab. Dis. 10:174?187.