Silent β-Thalassemia Associated with Hb Knossos β27 (B9) Ala→Ser in Algeria
- 1 January 1983
- journal article
- research article
- Published by Taylor & Francis in Hemoglobin
- Vol. 7 (6), 555-561
- https://doi.org/10.3109/03630268309027935
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- "Silent" nucleotide substitution in a beta+-thalassemia globin gene activates splice site in coding sequence RNA.Proceedings of the National Academy of Sciences, 1983
- Specific transcription and RNA splicing defects in five cloned β-thalassaemia genesNature, 1983
- Abnormal RNA processing due to the exon mutation of βE-globin geneNature, 1982
- Structural study of hemoglobin Knossos, β27 (B9) Ala→SerFEBS Letters, 1982
- ‘Silent’ β-thalassaemia caused by a ‘silent’ β-chain mutant: the pathogenesis of a syndrome of thalassaemia intermediaBritish Journal of Haematology, 1982
- A catalogue of splice junction sequencesNucleic Acids Research, 1982
- Globin Chain Electrophoresis: a New Approach to the Determination of the Gγ/Aγ Ratio in Fetal Haemoglobin and to Studies of Globin SynthesisBritish Journal of Haematology, 1980