Heterogeneity of βs gene haplotypes in patients with sickle cell disease (SCD) in Oman: A review of relevant publications

Sickle cell disease (SCD), caused by a mutation in the β-globin gene HBB, is widely distributed in malaria endemic regions. The prevalence of sickle cell trait and disease reaches up to 4.8–6% and 0.2% respectively, which is the highest among the Arab Gulf states. Omani population represents a varia...

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Detalles Bibliográficos
Autores principales: Al-Mashaikhi, Nawal, Al-Rawas, Abdulhakim, Wali, Yasser, Soliman, Ashraf, Khater, Doaa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2022
Materias:
Advances in Hemoglobinopathies (Editor: Ashraf T Soliman)
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534257/
https://www.ncbi.nlm.nih.gov/pubmed/36043956
http://dx.doi.org/10.23750/abm.v93i4.13336

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534257/
https://www.ncbi.nlm.nih.gov/pubmed/36043956
http://dx.doi.org/10.23750/abm.v93i4.13336

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