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Article

Molecular Characterization of δ-Thalassemia in Iran.

Hemoglobin - 1 Jan 2016

Kordafshari Alireza, Amirian Azam, Zeinali Sirous, Valaei Atefeh, Maryami Fereshteh, Karimipoor Morteza

Abstract excerpt

δ-Thalassemia (δ-thal) (OMIM #142000) resulting from mutations on the HBD gene usually has no clinical consequences. However, it may cause the misdiagnosis of β-thalassemia (β-thal) carriers by lowering the Hb A2 level to the normal range. Therefore, a study for δ-thal should be considered as a step in the detection of at-risk couple in our region. The aim of the present study was to characterize the mutations of...

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Source

Identifiers

PMID: 26754299
DOI: 10.3109/03630269.2015.1092982

Genes

HBD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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