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Article

β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey.

Hemoglobin - 1 Jul 2020

Guzelgul Figen, Seydel G Seyda, Aksoy Kiymet

Abstract excerpt

β-Thalassemia (β-thal) is one of the most common genetic disorders in Turkey. In this study, we investigated the mutations and frequency of β-thal at the molecular level in pediatric β-thal patients in the Çukurova region. The β-thal mutations of 52 cases were analyzed. An automated blood cell counter was used for hematological data. Cellulose acetate electrophoresis and high performance liquid chromatography...

Topics

Adolescent
Alleles
Child
Chromatography, High Pressure Liquid
Codon
Erythrocyte Indices
Female
Gene Frequency
Genotype
Humans
Male
Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Population Surveillance

Turkey

beta-Globins

beta-Thalassemia

Source

Identifiers

PMID: 32664780
DOI: 10.1080/03630269.2020.1792489

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-32664780-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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