Heterogeneity of erythrocyte catalase in Japanese-type acatalasemia by electrofocusing

Author:

Ogata Masana,Mizugaki Junko

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine,Ecology, Evolution, Behavior and Systematics,Biochemistry

Reference12 articles.

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.

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