Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation
- 1 June 1988
- Vol. 53 (6) , 881-885
- https://doi.org/10.1016/s0092-8674(88)90349-2
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- A new human species of aldolase A mRNA from fibroblastsEuropean Journal of Biochemistry, 1987
- Viability of λ phages carrying a perfect palindrome in the absence of recombination nucleasesNature, 1983
- pEMBL: a new family of single stranded plasmidsNucleic Acids Research, 1983
- Molecular studies of liver aldolase B in hereditary fructose intolerance using blotting and immunological techniquesAnnals of Human Genetics, 1982
- A bacteriophage lambda vector for cloning large DNA fragments made with several restriction enzymesGene, 1980
- Antibody activation of mutant human fructosediphosphate aldolase B in liver extracts of patients with hereditary fructose intoleranceBiochemical and Biophysical Research Communications, 1974
- Absence of Renal Fructose-1-phosphate Aldolase Activity in Hereditary Fructose IntoleranceNature, 1967
- Anomalie de l’aldolase hépatique dans l’intolérance au fructoseEnzymologia Biologica Et Clinica, 1961
- IDIOSYNCRASY TO FRUCTOSEThe Lancet, 1956
- Le metabolisme du fructose-1-phosphate dans le foieBiochimica et Biophysica Acta, 1953