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Article

Beta-thalassaemia and sickle cell anaemia as paradigms of hypercoagulability.

British journal of haematology - 1 Oct 2007

Ataga Kenneth I, Cappellini Maria D, Rachmilewitz Eliezer A

Abstract excerpt

Thalassaemia and sickle cell disease (SCD) represent the most common forms of hereditary haemolytic anaemia and result from a partial or complete lack of synthesis of one of the major alpha- or beta-globin chains of haemoglobin A or from a single amino acid mutation (beta(6Glu-->Val)) of the beta...

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Source

Identifiers

PMID: 17854302
DOI: 10.1111/j.1365-2141.2007.06740.x

Genes

SCD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17854302-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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