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Article

The molecular pathology of beta-thalassemia in Turkey: the Boğaziçi university experience.

Hemoglobin - 1 Jan 2007

Basak A Nazi

Abstract excerpt

The thalassemias are a diverse group of hemoglobin (Hb) disorders characterized by a reduced synthesis of the globin chains of Hb. Today, more than 200 mutations, affecting different levels of beta-globin gene expression, by a variety of mechanisms, are known to result in a beta-thalassemia (thal) phenotype. According to recent findings, the multilayered complexity in the phenotype of beta-thal is the result not...

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PMID: 17486506
DOI: 10.1080/03630260701296735

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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