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Molecular basis and diagnosis of thalassemia

Thalassemia is characterized by the impaired synthesis of globin chains due to disease-causing variants in α- or β-globin genes. In this review, we provide an overview of the molecular basis underlying α- and β-thalassemia, and of the current technologies used to characterize these disease-causing v...

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Detalles Bibliográficos
Autores principales:	Lee, Jee-Soo, Cho, Sung Im, Park, Sung Sup, Seong, Moon-Woo
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2021
Materias:	Review Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093999/ https://www.ncbi.nlm.nih.gov/pubmed/33935034 http://dx.doi.org/10.5045/br.2021.2020332

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