Triosephosphate isomerase deficiency: historical perspectives and molecular aspects
- 1 March 2000
- journal article
- review article
- Published by Elsevier in Best Practice & Research Clinical Haematology
- Vol. 13 (1) , 119-140
- https://doi.org/10.1053/beha.2000.0061
Abstract
No abstract availableKeywords
This publication has 60 references indexed in Scilit:
- Triosephosphate isomerase deficiency: Repetitive occurrence of point mutation in amino acid 104 in multiple apparently unrelated familiesAmerican Journal of Hematology, 1995
- Hereditary deficiency of triosephosphate isomerase in four unrelated familiesEuropean Journal of Clinical Investigation, 1979
- Triosephosphate isomerase deficiency with hemolytic anemia and severe neuromuscular disease. Familial and biochemical studies of a case found in SpainHuman Genetics, 1978
- Triose phosphate isomerase deficiencyBiochemical Medicine, 1977
- 12pter ? 12p 12.2: Possible assignment of human triose phosphate isomeraseHuman Genetics, 1977
- Evidence for Synteny between the Human Loci for Triose Phosphate Isomerase, Lactate Dehydrogenase-B, and Peptidase-B and the Regional Mapping of these Loci on Chromosome 12Cytogenetic and Genome Research, 1974
- Electrophoretic abnormality in triosephosphate isomerase deficiencyBiochemical and Biophysical Research Communications, 1968
- Hereditary hemolytic anemia with triosephosphate isomerase deficiencyThe American Journal of Medicine, 1966
- Erythrocyte triosephosphate isomerase deficiencyThe Journal of Pediatrics, 1965
- Hereditary Hemolytic Anemia with Triosephosphate Isomerase DeficiencyNew England Journal of Medicine, 1965