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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...

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Detalhes bibliográficos
Main Authors: Jones, R.W., Old, J.M., Trent, R.J., Clegg, J.B., Weatherall, D.J.
Formato: Artigo
Idioma:Inglês
Publicado em: 1981
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC327644/
https://ncbi.nlm.nih.gov/pubmed/6278449
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