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Article

Hb TAYBE: clinical and morphological findings IN 43 patients.

European journal of haematology - 1 Aug 2016

Koren Ariel, Levin Carina, Zalman Luci, Palmor Haya, Filon Dvora, Chubar Evgeny, Resnitzky Peretz, Bennett Michael

Abstract excerpt

UNLABELLED: Hereditary sequence variants in globin genes are usually silent and are rarer in α-globin chains than β-globin chains. Some may lead to an unstable protein with a hemolytic or thalassemic phenotype. Hb Taybe is an unstable α-chain hemoglobin variant caused by the deletion of a threonine residue at codon 38 or 39 of the α1 globin gene. This deletion results in a structural abnormality that affects the...

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PMID: 26519868
DOI: 10.1111/ejh.12694

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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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