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Article

Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype.

Hemoglobin - 1 Jan 2007

Harteveld Cornelis L, van Helden Willem C H, Boxma George L, van Delft Peter, Bakker-Verweij Margaretha, Wajcman Henri, Zanella-Cleon Isabelle, Becchi Michel, Giordano Piero C

Abstract excerpt

A 52-year-old Dutch male was referred to our laboratory for hemoglobinopathy analysis because of persistent microcytic hypochromic parameters and moderate erythrocytosis in the absence of iron deficiency. The hemoglobin (Hb) pattern was normal and breakpoint polymerase chain reaction (PCR) exclud...

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Identifiers

PMID: 17654069
DOI: 10.1080/03630260701459374

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17654069-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype.PMID 17654069Read ↗

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