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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...

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PMID: 18932071
DOI: 10.1080/03630260802341851

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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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