The major defect in Ashkenazi Jews with Tay-Sachs disease is an insertion in the gene for the alpha-chain of beta-hexosaminidase.
Open Access
- 1 December 1988
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 263 (35) , 18587-18589
- https://doi.org/10.1016/s0021-9258(18)37323-x
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Identification of an altered splice site in Ashkenazi Tay-Sachs diseaseNature, 1988
- A splicing defect due to an exon-intron junctional mutation results in abnormal β-hexosaminidase α chain mRNAs in Ashkenazi Jewish patients with Tay-Sachs diseaseBiochemical and Biophysical Research Communications, 1988
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- [21] Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reactionPublished by Elsevier ,1987
- Different Mutations in Ashkenazi Jewish and Non-Jewish French Canadians with Tay-Sachs DiseaseScience, 1986
- THE MUTATION AND POLYMORPHISM OF THE HUMAN β-GLOBIN GENE AND ITS SURROUNDING DNAAnnual Review of Genetics, 1984
- The Biochemical Basis of GangliosidosesNeuropediatrics, 1984
- Rapid purification of plasmid DNA by a single centrifugation in a two-step cesium chloride-ethidium bromide gradientBiochemical and Biophysical Research Communications, 1983
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1983
- Recognition and receptor-mediated uptake of a lysosomal enzyme, α-l-iduronidase, by cultured human fibroblastsCell, 1977