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Article

Molecular and Hematological Analysis of Alpha- and Beta-Thalassemia in a Cohort of Mexican Patients.

Genetic testing and molecular biomarkers - 1 Mar 2021

Rizo-de la Torre Lourdes Del Carmen, Rentería-López Víctor Manuel, Sánchez-López Josefina Yoaly, Magaña-Torres María Teresa, Ibarra-Cortés Bertha, Perea-Díaz Francisco Javier

Abstract excerpt

Introduction: Alpha- and beta-thalassemia are caused by reduced or absent synthesis of hemoglobin (Hb) subunits α and/or β. HBA2, HBA1, and HBB mutations are the main cause of thalassemias. The aim of this article is to analyze molecular and hematological features of α- and β-thal in a cohort of Mexican patients. Methods: One hundred forty-one thalassemia patients were studied. Peripheral blood was collected for...

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PMID: 33734896
DOI: 10.1089/gtmb.2020.0276

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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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