Hematologically Important Mutations: Red Cell Pyruvate Kinase
- 1 December 1996
- journal article
- Published by Elsevier in Blood Cells, Molecules, and Diseases
- Vol. 22 (3) , 259-264
- https://doi.org/10.1006/bcmd.1996.0107
Abstract
No abstract availableThis publication has 17 references indexed in Scilit:
- Five unknown mutations in the LR pyruvate kinase gene associated with severe hereditary nonspherocytic haemolytic anaemia in FranceBritish Journal of Haematology, 1996
- Mutations in pyruvate kinaseHuman Mutation, 1996
- Study of the Molecular Defects in Pyruvate Kinase Deficient Patients Affected by Nonspherocytic Hemolytic AnemiaBlood Cells, Molecules, and Diseases, 1995
- Molecular study of pyruvate kinase deficient patients with hereditary nonspherocytic hemolytic anemia.Journal of Clinical Investigation, 1995
- Compound Heterozygous Mutations Affecting Both Hepatic and Erythrocyte Isozymes of Pyruvate KinaseBiochemical and Biophysical Research Communications, 1995
- Hereditary hemolytic anemia caused by diverse point mutations of pyruvate kinase gene found in Japan and Hong KongBlood, 1994
- Mutations in the R-type pyruvate kinase gene and altered enzyme kinetic properties in patients with hemolytic anemia due to pyruvate kinase deficiencyAnnals of Hematology, 1994
- Analysis of pyruvate kinase-deficiency mutations that produce nonspherocytic hemolytic anemia.Proceedings of the National Academy of Sciences, 1993
- Pyruvate kinase deficiency: Historical perspective and recent progress of molecular geneticsAmerican Journal of Hematology, 1993
- Point mutations in the L-type pyruvate kinase gene of two children with hemolytic anemia caused by pyruvate kinase deficiency [see comments]Blood, 1991