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Molecular basis for dominantly inherited inclusion body beta-thalassemia.

Analysis of the molecular basis of dominantly inherited beta-thalassemia in four families has revealed different mutations involving exon 3 of the beta-globin gene. It is suggested that the phenotypic difference between this condition and the more common recessive forms of beta-thalassemia lies main...

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Publicado no:Proc Natl Acad Sci U S A
Principais autores: Thein, S L, Hesketh, C, Taylor, P, Temperley, I J, Hutchinson, R M, Old, J M, Wood, W G, Clegg, J B, Weatherall, D J
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 1990
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC54016/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1971109/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.87.10.3924
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