Biochemical and molecular analysis of the beta-globin gene and LCR region on Saudi β-thalassemia patients

INTRODUCTION: Beta-thalassemias are a group of inherited blood disorders caused by reduced or absent synthesis of beta chain of hemoglobin resulting in variable phenotypes ranging from clinically asymptomatic individuals to severe anemia symptoms. The objective of this study is to screen for the who...

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Detalles Bibliográficos
Autores principales: Alafari, Hayat, Alenzi, Faris Q.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569122/
https://www.ncbi.nlm.nih.gov/pubmed/33100871
http://dx.doi.org/10.1016/j.sjbs.2020.08.044

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569122/
https://www.ncbi.nlm.nih.gov/pubmed/33100871
http://dx.doi.org/10.1016/j.sjbs.2020.08.044

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