Three cases of hereditary hemolytic anemia with pyrimidine 5?-nucleotidase deficiency in a Japanese family

Author:

Miwa Shiro,Nakashima Koji,Fujii Hisaichi,Matsumoto Minoru,Nomura Koichiro

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference6 articles.

1. Ben-Bassat, I., Brok-Simoni, F., Kende, G., Holtzmann, F., Ramot, B.: The family with red cell pyrimidine 5?-nucleotidase deficiency. Blood 47, 919?922 (1976)

2. Beutler, E.: Red cell metabolism; a manual of biochemical methods, 2nd ed. New York: Grune and Stratton 1975

3. Oda, S., Tanaka, K. R.: Metabolic studies in erythrocyte pyrimidine 5?-nucleotidese deficiency. Clin. Res. 24, 149a (1976)

4. Rochant, H., Dreyfus, B., Rosa, R., Boiron, M.: First case of pyrimidine 5?-nucleotidase deficiency in a male. International Society of Haematology, European and African Division, Third Meeting, London, August 24?28 (1975). Abstract 1:19

5. Valentine, W. N., Fink, K., Paglia, D. E., Harris, S. R., Adams, W. S.: Hereditary hemolytic anemia with human erythrocyte pyrimidine 5?-nucleotidase deficiency. J. Clin. Invest. 54, 866?879 (1974)

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