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Article

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

Haematologica - 1 Sept 2021

Kountouris Petros, Michailidou Kyriaki, Christou Soteroula, Hadjigavriel Michael, Sitarou Maria, Kolnagou Anita, Kleanthous Marina, Telfer Paul

Abstract excerpt

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 genotype with survival in a cohort study in the four thalassemia centres in Cyprus. HBB genotype was classified as severe...

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Identifiers

PMID: 32732363
DOI: 10.3324/haematol.2020.260224
PMCID: PMC8409026

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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