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Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients

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Hemoglobinopathies, inherited disorders of hemoglobin (Hb), are the most common hereditary monogenic diseases of the red cell in the world. Few studies have been conducted on hemoglobinopathies in Mauritania. Therefore,… Click to show full abstract

Hemoglobinopathies, inherited disorders of hemoglobin (Hb), are the most common hereditary monogenic diseases of the red cell in the world. Few studies have been conducted on hemoglobinopathies in Mauritania. Therefore, the aim of this work is to establish the molecular and epidemiological basis of hemoglobinopathies in a cohort of Mauritanian patients and to determine the haplotype of the β‐globin gene cluster in sickle cell subjects.

Keywords: study hemoglobinopathies; mauritanian patients; epidemiological molecular; molecular study; hemoglobinopathies mauritanian

Journal Title: Molecular Genetics & Genomic Medicine
Year Published: 2022

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