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Article

Molecular basis of thalassemia intermedia in Iran.

Hemoglobin - 1 Jan 2008

Akbari Mohammad T, Izadi Pantea, Izadyar Mina, Kyriacou Kyriacou, Kleanthous Marina

Abstract excerpt

Thalassemia intermedia shows considerable heterogenity in phenotype and molecular basis. The aim of this study was to evaluate the prevalence and effect of different beta-globin mutations, alpha-globin defects and (G)gamma XmnI polymorphisms in Iranian patients. Forty-five Iranian patients with clinical criteria of thalassemia intermedia were studied. The molecular background of the diseases was investigated. The...

Topics

Adolescent
Adult
Child
Child, Preschool
Gene Frequency
Genotype
Humans
Infant
Iran
Middle Aged
Polymorphism, Genetic
Young Adult

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

alpha-Globins

beta-Globins

beta-Thalassemia

Source

Identifiers

PMID: 18932071
DOI: 10.1080/03630260802341851

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-18932071-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

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

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