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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...

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Detalhes bibliográficos
Publicado no:Saudi J Biol Sci
Main Authors: Alafari, Hayat, Alenzi, Faris Q.
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7569122/
https://ncbi.nlm.nih.gov/pubmed/33100871
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.sjbs.2020.08.044
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