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The deletion of the distal CCAAT box region of the A gamma-globin gene in black HPFH abolishes the binding of the erythroid specific protein NFE3 and of the CCAAT displacement protein.

Non-deletion Hereditary Persistence of Fetal Hemoglobin (HPFH) is characterized by great elevation of the synthesis, in adult age, of fetal hemoglobin (HbF), of either the A gamma or G gamma type. Strong genetic evidence indicates point mutations in the G gamma- or A gamma-globin promoter as respons...

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Publicat a:Nucleic Acids Res
Autors principals: Mantovani, R, Superti-Furga, G, Gilman, J, Ottolenghi, S
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 1989
Accés en línia:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC318359/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2476717/
https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/17.16.6681
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