Characterisation of a new alpha thalassemia 1 defect due to a partial deletion of the alpha globin gene complex.
A new deletion causing alpha thalassemia has been characterised in a Greek family. Detailed mapping of the alpha gene complex shows that the deletion extends for 5.2 kb and removes the whole of the alpha 2 gene and the 5' end of the alpha 1 gene. The affected chromosome, therefore produces no normal...
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| Gepubliceerd in: | Nucleic Acids Res |
|---|---|
| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
1980
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| Online toegang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC324266/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6255436/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/8.21.4889 |
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