Sickle Cell Anemia Screening in Newborns and Analysis of Haplotypes in Patients from Santiago Island, Cape Verde

Sickle cell anemia (SCA) results from a mutation in the β-globin gene, leading to the production of mutant hemoglobin, known as hemoglobin S (HbS). Despite being a genetic disorder, the phenotype of SCA can be influenced by the level of fetal hemoglobin (HbF), which is associated with beta S-globin...

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Bibliographic Details
Main Authors: Ariana Freire, Laura Charola-Ramos, Elisa González-Guerra, João Gonçalves, Vanusa Rocha, Vera Afreixo, Enrique Martínez-Carretero, José M. Raya
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:Anemia
Online Access:http://dx.doi.org/10.1155/2024/1687917
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