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Article

Molecular characterization of thalassemia intermedia associated with HPFH-6/beta-thalassemia and HPFH-6/Hb E in Thai patients.

Acta haematologica - 1 Jan 2002

Fucharoen Supan, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Surapot Satja

Abstract excerpt

We report the molecular and hematological characterizations of thalassemia caused by interactions of the hereditary persistence of fetal hemoglobin (HPFH)-6 with beta-thalassemia in 2 Thai patients and the HPFH-6 with Hb E in another Thai patient. Marked hypochromic microcytosis, characteristics...

Topics

Aged
Child
Child, Preschool
Codon
Fetal Hemoglobin
Hemoglobin E
Humans
Male
Mutation
Thalassemia
beta-Thalassemia

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 12373089
DOI: 10.1159/000064707

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-12373089-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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