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Article

Dinucleotide deletion in -alpha3.7 allele causes a severe form of alpha+ thalassaemia.

European journal of haematology - 1 Aug 2003

Viprakasit Vip, Ayyub Helena, May Alison

Abstract excerpt

We describe a family of Italian origin in which the father and his two children had hypochromia and microcytosis with normal iron status. All individuals underwent an uneventful clinical course and required no treatment. To investigate the molecular basis of this phenotype, which is a prerequisite for further genetic counselling, we revealed that all affected family members are carriers of a common form of alpha+...

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Identifiers

PMID: 12890155
DOI: 10.1034/j.1600-0609.2003.00106.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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