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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| Autori principali: | , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Ferrata Storti Foundation
2020-07-01
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| Serie: | Haematologica |
| Accesso online: | https://haematologica.org/article/view/9831 |
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