Molecular heterogeneity of β‐thalassemia variants in the Eastern region of Morocco

Molecular heterogeneity of β‐thalassemia variants in the Eastern region of Morocco

Abstract Background β‐thalassemia syndromes are the most common hereditary blood disorders in the world and are recognized as a major health problem in Morocco. They are characterized by the reduction or the absence of β‐globin chain synthesis. The severity of the disease depends on the nature of th...

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Bibliographic Details
Main Authors: Ihab Belmokhtar, Saida Lhousni, Mounia Elidrissi Errahhali, Ayad Ghanam, Manal Elidrissi Errahhali, Zaina Sidqi, Meryem Ouarzane, Majida Charif, Mohammed Bellaoui, Redouane Boulouiz, Noufissa Benajiba
Format: Article
Language:English
Published: Wiley 2022-08-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
BRO Biobank
hemoglobin
molecular profile
morocco
variant
β‐thalassemia
Online Access:https://doi.org/10.1002/mgg3.1970

Internet

https://doi.org/10.1002/mgg3.1970

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