β Thalassemia due to a novel mutation in IVS 1 sequence donor site consensus sequence creating a restriction site
Open Access
- 1 September 1986
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 139 (2), 709-713
- https://doi.org/10.1016/s0006-291x(86)80048-1
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- DNA polymorphism and molecular pathology of the human globin gene clustersHuman Genetics, 1985
- Quantification of the close association between DNA haplotypes and specific β-thalassaemia mutations in MediterraneansNature, 1984
- Molecular characterization of seven beta-thalassemia mutations in Asian Indians.The EMBO Journal, 1984
- Four new haplotypes observed in Algerian ?-thalassemia patientsHuman Genetics, 1983
- Specific transcription and RNA splicing defects in five cloned β-thalassaemia genesNature, 1983
- Evidence for multiple origins of the beta E-globin gene in Southeast Asia.Proceedings of the National Academy of Sciences, 1982
- Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene clusterNature, 1982
- A nucleotide change at a splice junction in the human beta-globin gene is associated with beta 0-thalassemia.Proceedings of the National Academy of Sciences, 1981
- The nucleotide sequence of the human β-globin geneCell, 1980
- DNA sequencing with chain-terminating inhibitorsProceedings of the National Academy of Sciences, 1977