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

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 the varian...

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Detalles Bibliográficos
Autores principales: Belmokhtar, Ihab, Lhousni, Saida, Elidrissi Errahhali, Mounia, Ghanam, Ayad, Elidrissi Errahhali, Manal, Sidqi, Zaina, Ouarzane, Meryem, Charif, Majida, Bellaoui, Mohammed, Boulouiz, Redouane, Benajiba, Noufissa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356555/
https://www.ncbi.nlm.nih.gov/pubmed/35615994
http://dx.doi.org/10.1002/mgg3.1970

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356555/
https://www.ncbi.nlm.nih.gov/pubmed/35615994
http://dx.doi.org/10.1002/mgg3.1970

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