Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics

We described the clinical, laboratory and molecular characteristics of individuals with Hb S (HBB: c.20A>T)/β-thalassemia (Hb S/β-thal) participating in the Recipient Epidemiology and Donor Evaluation Study (REDS-III) Brazil Sickle Cell Disease cohort. HBB gene sequencing was performed to genotyp...

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Vydáno v:Hemoglobin
Hlavní autoři: Belisário, André R., Carneiro-Proietti, Anna B., Sabino, Ester Cerdeira, Araújo, Aderson, Loureiro, Paula, Máximo, Cláudia, Flor-Park, Miriam V., Rodrigues, Daniela DOW, Ozahata, Mina Cintho, McClure, Christopher, Mota, Rosimere Afonso, Moura, Isabel C. Gomes, Custer, Brian, Kelly, Shannon
Médium: Artigo
Jazyk:Inglês
Vydáno: 2020
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7225056/
https://ncbi.nlm.nih.gov/pubmed/32172616
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/03630269.2020.1731530
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