1. Aebi, H., and Wyss, S. R. (1977). Acatalasemia. In Stanburg, J. B., Wyngaarden, J. B., and Frederickson, D. S. (eds.), The Metabolic Basis of Inherited Disease 4th ed., McGraw-Hill, New York, p. 1792.
2. Aebi, H., Wyss, S. R., and Scherz, B. (1975). Heterogeneity of human erythrocyte catalase. In Markert, C. L. (ed.), Isozymes, Vol. I. Molecular Structure Academic Press, New York-San Francisco-London, p. 227.
3. Aebi, H., Wyss, S. R., and Scherz, B. (1977). Unstable mutants and molecular hybrids in enzyme deficiency conditions. Acta Biol. Med. Germ. 36735.
4. Aebi, H., Wyass, S. R., Scherz, B., and Gross, J. (1976). Properties of erythrocyte catalase from homozygotes and heterozygotes for Swiss-type acatalasemia. Biochem. Genet. 14791.
5. Ogata, M., and Mizugaki, J. (1978). Residual catalase in Japanese type acatalasemia. Cell Struct. Funct. 3279.