Skip to main content
PMC home page
American Journal of Human Genetics logoLink to American Journal of Human Genetics
letter
. 1995 Apr;56(4):1002–1005.

Diverse mutations in the aldolase B gene that underlie the prevalence of hereditary fructose intolerance.

M Ali, T M Cox
PMCID: PMC1801191  PMID: 7717389

Full text

PDF
1002

Images in this article

1003Figure 2
on p.1003

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ali M., Rosien U., Cox T. M. DNA diagnosis of fatal fructose intolerance from archival tissue. Q J Med. 1993 Jan;86(1):25–30. [PubMed] [Google Scholar]
  2. CORNBLATH M., ROSENTHAL I. M., REISNER S. H., WYBREGT S. H., CRANE R. K. HEREDITARY FRUCTOSE INTOLERANCE. N Engl J Med. 1963 Dec 12;269:1271–1278. doi: 10.1056/NEJM196312122692401. [DOI] [PubMed] [Google Scholar]
  3. Cox T. M., Camilleri M., O'Donnell M. W., Chadwick V. S. Pseudodominant transmission of fructose intolerance in an adult and three offspring: Heterozygote detection by intestinal biopsy. N Engl J Med. 1982 Aug 26;307(9):537–540. doi: 10.1056/NEJM198208263070906. [DOI] [PubMed] [Google Scholar]
  4. Cox T. M. Iatrogenic deaths in hereditary fructose intolerance. Arch Dis Child. 1993 Oct;69(4):413–415. doi: 10.1136/adc.69.4.413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cox T. M., O'Donnell M. W., Camilleri M. Allelic heterogeneity in adult hereditary fructose intolerance. Detection of structural mutations in the aldolase B molecule. Mol Biol Med. 1983 Nov;1(4):393–400. [PubMed] [Google Scholar]
  6. Cross N. C., Cox T. M. Molecular analysis of aldolase B genes in the diagnosis of hereditary fructose intolerance in the United Kingdom. Q J Med. 1989 Nov;73(271):1015–1020. [PubMed] [Google Scholar]
  7. Cross N. C., Tolan D. R., Cox T. M. Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation. Cell. 1988 Jun 17;53(6):881–885. doi: 10.1016/s0092-8674(88)90349-2. [DOI] [PubMed] [Google Scholar]
  8. Cross N. C., de Franchis R., Sebastio G., Dazzo C., Tolan D. R., Gregori C., Odievre M., Vidailhet M., Romano V., Mascali G. Molecular analysis of aldolase B genes in hereditary fructose intolerance. Lancet. 1990 Feb 10;335(8685):306–309. doi: 10.1016/0140-6736(90)90603-3. [DOI] [PubMed] [Google Scholar]
  9. Dazzo C., Tolan D. R. Molecular evidence for compound heterozygosity in hereditary fructose intolerance. Am J Hum Genet. 1990 Jun;46(6):1194–1199. [PMC free article] [PubMed] [Google Scholar]
  10. FROESCH E. R., WOLF H. P., BAITSCH H., PRADER A., LABHART A. Hereditary fructose intolerance. An inborn defect of hepatic fructose-1-phosphate splitting aldolase. Am J Med. 1963 Feb;34:151–167. doi: 10.1016/0002-9343(63)90050-0. [DOI] [PubMed] [Google Scholar]
  11. HERS H. G., JOASSIN G. [Anomaly of hepatic aldolase in intolerance to fructose]. Enzymol Biol Clin (Basel) 1961;1:4–14. [PubMed] [Google Scholar]
  12. Landau B. R., Marshall J. S., Craig J. W., Hostetler K. Y., Genuth S. M. Quantitation of the pathways of fructose metabolism in normal and fructose-intolerant subjects. J Lab Clin Med. 1971 Oct;78(4):608–618. [PubMed] [Google Scholar]
  13. Nagamine C. M., Chan K., Lau Y. F. A PCR artifact: generation of heteroduplexes. Am J Hum Genet. 1989 Aug;45(2):337–339. [PMC free article] [PubMed] [Google Scholar]
  14. Rampa M., Froesch E. R. Eleven cases of hereditary fructose intolerance in one Swiss family with a pair of monozygotic and of dizygotic twins. Helv Paediatr Acta. 1981 Sep;36(4):317–324. [PubMed] [Google Scholar]
  15. Rosenthal A., Charnock-Jones D. S. New protocols for DNA sequencing with dye terminators. DNA Seq. 1992;3(1):61–64. doi: 10.3109/10425179209039697. [DOI] [PubMed] [Google Scholar]
  16. Ruano G., Kidd K. K. Coupled amplification and sequencing of genomic DNA. Proc Natl Acad Sci U S A. 1991 Apr 1;88(7):2815–2819. doi: 10.1073/pnas.88.7.2815. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Santamaria R., Scarano M. I., Esposito G., Chiandetti L., Izzo P., Salvatore F. The molecular basis of hereditary fructose intolerance in Italian children. Eur J Clin Chem Clin Biochem. 1993 Oct;31(10):675–678. doi: 10.1515/cclm.1993.31.10.675. [DOI] [PubMed] [Google Scholar]
  18. Tolan D. R., Brooks C. C. Molecular analysis of common aldolase B alleles for hereditary fructose intolerance in North Americans. Biochem Med Metab Biol. 1992 Aug;48(1):19–25. doi: 10.1016/0885-4505(92)90043-x. [DOI] [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES