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Article

Genotype-phenotype correlation in Iranian patients with Hb H disease.

Hemoglobin - 1 Jan 2011

Ebrahimkhani Saedieh, Azarkeivan Azita, Bayat Nooshin, Houry-Parvin Mahdieh, Jalil-Nejad Sayeh, Zand Shima, Golkar Zahra, Hadavi Valeh, Imanian Hashem, Oberkanins Christian, Najmabadi Hossein

Abstract excerpt

Thalassemia is the most common genetic disorder in Iran. Some α-globin genotypes leading to Hb H disease may cause severe anemia and dependence on regular blood transfusions. In this study, 40 patients were analyzed for the molecular basis and the genotype-phenotype correlation of Hb H disease in Iran. α-Globin molecular analysis was performed by polymerase chain reaction (PCR) followed by agarose gel...

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Identifiers

PMID: 21250880
DOI: 10.3109/03630269.2010.546314

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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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