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Article

Nondeletional Hb Queens Park [α32(B13)Met→Lys]/Hb H (β4) disease.

Hemoglobin - 1 Jan 2012

Sroymora Suravee, Jindadamrongwech Sumalee, Butthep Punnee, Chuncharunee Suporn

Abstract excerpt

A rare nondeletional α-thalassemia-2 (α-thal-2) allele was identified in a Thai boy with Hb H (β4) disease. The proband has α-thal-1 (- -(SEA) type) together with a non productive Hb Queens Park (HBA1:c.98T>A) [α32(B13)Met→Lys] α1-globin variant. No abnormal hemoglobin (Hb) fraction was detected by high performance liquid chromatography (HPLC). The clinical effect of this mutation in the proband was comparable to...

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Source

Identifiers

PMID: 22384838
DOI: 10.3109/03630269.2012.658939

Genes

HBA1
SEA

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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