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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...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Saudi J Biol Sci
Päätekijät: Alafari, Hayat, Alenzi, Faris Q.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Elsevier 2020
Aiheet:
Linkit: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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