Responses of β-thalassemia and compound heterozygote of Sickle/βthalassemia of BCL11A Gene Polymorphism in Pakistani Patients

BACKGROUND AND OBJECTIVE: Beta-thalassemia major (β-Thal) and compound heterozygote of Sickle β-thalassemia (S-β Thal) are hereditary autosomal recessive disorders resulting from mutations or deletion in β-globin gene cluster. Patients with increased HbF levels having polymorphism at BCL11A site loc...

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Detalles Bibliográficos
Autores principales: Soomro, Nayab, Wahid, Mohsin, Mehmood, Mehreen, Danish, Syed Hasan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626103/
https://www.ncbi.nlm.nih.gov/pubmed/37936787
http://dx.doi.org/10.12669/pjms.39.6.7183

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626103/
https://www.ncbi.nlm.nih.gov/pubmed/37936787
http://dx.doi.org/10.12669/pjms.39.6.7183

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