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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...
Autores principales: | Alafari, Hayat, Alenzi, Faris Q. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
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 |
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