Restriction mapping of a new deletion responsible for (G)γ(δβ)(o) thalassaemia
DNA from individuals heterozygous for (G)γ(δβ)(o) thalassaemia has been studied by restriction endonuclease analysis. The results reveal a new molecular defect associated with this condition. A total of three defects is now responsible for the one single phenotype, thereby emphasising the complex re...
Uloženo v:
| Vydáno v: | Nucleic Acids Res |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
1981
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC327644/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6278449/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/9.24.6813 |
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