Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?

The hematological phenotypes of several Mediterranean patients with delta beta-thalassemia and hereditary persistence of fetal hemoglobin have been characterized. Although clinical and hematological characteristics are essentially superimposable in all heterozygous delta beta-thalassemics, these pat...

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Detalhes bibliográficos

Publicado no:	Proc Natl Acad Sci U S A
Principais autores:	Ottolenghi, S, Giglioni, B, Taramelli, R, Comi, P, Mazza, U, Saglio, G, Camaschella, C, Izzo, P, Cao, A, Galanello, R, Gimferrer, E, Baiget, M, Gianni, A M
Formato:	Artigo
Idioma:	Inglês
Publicado em:	National Academy of Sciences 1982
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC346190/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/6179097/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.79.7.2347
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