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Article

Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian population.

European journal of haematology - 1 Jun 2014

Mayuranathan Thiyagaraj, Rayabaram Janakiram, Das Reena, Arora Neeraj, Edison Eunice S, Chandy Mammen, Srivastava Alok, Velayudhan Shaji R

Abstract excerpt

OBJECTIVES: Hereditary persistence of foetal haemoglobin (HPFH) and (δβ)(0) -thalassaemia are conditions caused by large deletions that involve δ- and β-globin genes in the β-globin cluster, and they are characterized by increased haemoglobin (HbF) levels in adults. Significant phenotypic diversity is observed between the different mutations that cause these conditions. Molecular characterization of these...

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PMID: 24471888
DOI: 10.1111/ejh.12276

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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