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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...

Topics

Amino Acid Substitution
Gene Frequency
Globins
Homozygote
Humans
Incidence
Mutation
Polymorphism, Single Nucleotide
Turkey
beta-Thalassemia

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 17486506
DOI: 10.1080/03630260701296735

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-17486506-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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