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Article

Haemoglobin Lleida: a new alpha 2-globin variant (12 bp deletion) with mild thalassaemic phenotype.

British journal of haematology - 1 Sept 1996

Ayala S, Colomer D, Pujades A, Aymerich M, Vives Corrons J L

Abstract excerpt

Molecular studies of alpha-thalassaemias have revealed defects at different steps in the process of alpha-gene expression. It is not surprising, therefore, that in some cases a single mutation or small deletion can result in a structurally abnormal haemoglobin that produces the alpha-thalassaemia phenotype. In this report we describe a new unstable alpha-globin variant, Hb Lleida, in a Spanish patient with...

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Identifiers

PMID: 8826886
DOI: 10.1046/j.1365-2141.1996.d01-1840.x

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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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Haemoglobin Lleida: a new alpha 2-globin variant (12 bp deletion) with mild thalassaemic phenotype.PMID 8826886Read ↗

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Hb Bronte or alpha93(FG5)Val-->Gly: a new unstable variant of the alpha2-globin gene, associated with a mild alpha(+)-thalassemia phenotype.Semantic proximity Read ↗

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Hb Jambol: a new hyperunstable hemoglobin causing severe hemolytic anemia.Semantic proximity Read ↗

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A new stable alpha chain variant: Hb Basel [alpha14(A12)Trp-->Leu (alpha1)].Semantic proximity Read ↗

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