Effect of HBB genotype on survival in a cohort of transfusion-dependent thalassemia patients in Cyprus

Initiation of regular transfusion in transfusion-dependent thalassemia (TDT) is based on the assessment of clinical phenotype. Pathogenic HBB variants causing β-thalassemia are important determinants of phenotype and could be used to aid decision-making. We investigated the association of HBB genoty...

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Detalles Bibliográficos
Autores principales: Kountouris, Petros, Michailidou, Kyriaki, Christou, Soteroula, Hadjigavriel, Michael, Sitarou, Maria, Kolnagou, Anita, Kleanthous, Marina, Telfer, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409026/
https://www.ncbi.nlm.nih.gov/pubmed/32732363
http://dx.doi.org/10.3324/haematol.2020.260224

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8409026/
https://www.ncbi.nlm.nih.gov/pubmed/32732363
http://dx.doi.org/10.3324/haematol.2020.260224

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