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Article

[Molecular bases of α-thalassemia in Argentina].

Medicina - 1 Jan 2015

Scheps Karen G, Francipane Liliana, Nash Abigail, Cerrone Gloria E, Copelli Silvia B, Varela Viviana

Abstract excerpt

The α-thalassemia is one of the most common hereditary disorders worldwide. Currently, molecular diagnostics is the only available tool to achieve an accurate diagnosis. The purpose of this study was to characterize the molecular bases of these syndromes in our environment and to establish genotype-phenotype associations. Through a combination of different molecular techniques and fluorescent in situ...

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PMID: 25919868

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CAMP

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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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