A new mutant erythrocyte pyrimidine 5'-nucleotidase characterized by fast electrophoretic mobility in a Chinese boy with chronic hemolytic anemia
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference9 articles.
1. Hereditary hemolytic anemia with human erythrocyte pyrimidine 5'-nucleotidase deficiency;Valentine;J Clin Invest,1974
2. Electrophoretic and kinetic studies of a mutant red cell pyrimidine 5'-nucleotidase;Fujii;Clin Chim Acta,1979
3. Electrophoretic and kinetic studies of a new mutant red cell pyrimidine 5'-nucleotidase;Vives Corrons;Enzyme,1983
4. Erythrocyte pyrimidine 5'-nucleotidase deficiency. Report of 2 new cases, with a review of the literature;Hansen;Scand J Haematol,1983
5. Three families with hereditary hemolytic anemia and pyrimidine 5'-nucleotidase deficiency: electrophoretic and kinetic studies;Hirono;Clin Chim Acta,1983
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Hereditary pyrimidine 5'-nucleotidase deficiency: from genetics to clinical manifestations;British Journal of Haematology;2006-04
2. Hereditary erythrocyte pyrimidine 5′-nucleotidase deficiency: A biochemical, genetic and clinical overview;Hematology;2006-02
3. Biochemical and genetic basis of red cell enzyme deficiencies;Best Practice & Research Clinical Haematology;2000-03
4. Hereditäre Membrandefekte und Enzymopathien roter Blutzellen;Monogen bedingte Erbkrankheiten 1;2000
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