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Article

Detection of the Hb Hoshida (HBB: C. 130 G > C) Variant in the Indian Population.

Hemoglobin - 1 May 2026

Sen Aditi, Dolai Tuphan Kanti

Abstract excerpt

Hemoglobinopathies, including thalassemias and structural hemoglobin variants, are among the most common monogenic disorders worldwide. In genetically heterogeneous populations such as India, screening programs occasionally detect rare hemoglobin variants that may mimic common abnormalities, leading to diagnostic uncertainty. During prenatal screening of an at-risk couple, we identified a rare β-globin gene...

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Identifiers

PMID: 42157746
DOI: 10.1080/03630269.2026.2671886

Genes

HBB

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 15 Oct 2026.

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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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