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miRNA Expression Associated with HbF in Saudi Sickle Cell Anemia

Background and Objectives: Sickle cell anemia (SCA) is a hereditary monogenic disease due to a single β-globin gene mutation that codes for the production of sickle hemoglobin. Its phenotype is modulated by fetal hemoglobin (HbF), a product of γ-globin genes. Exploring the molecules that regulate γ-...

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Detalles Bibliográficos
Autores principales:	Cyrus, Cyril, Vatte, Chittibabu, Al-Nafie, Awatif, Chathoth, Shahanas, Akhtar, Mohammed S., Darwish, Mohammed, Almohazey, Dana, AlDubayan, Saud H., Steinberg, Martin H., Al-Ali, Amein
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9611475/ https://www.ncbi.nlm.nih.gov/pubmed/36295630 http://dx.doi.org/10.3390/medicina58101470

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