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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Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: 1990
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC54016/
https://ncbi.nlm.nih.gov/pubmed/1971109
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