AB089. Prevalence of the most common β-globin gene mutations in Filipino β-thalassemia patients

BACKGROUND: Beta (β)-thalassemia is an autosomal recessive disorder characterized by reduced or absent β-globin chain synthesis resulting in decreased hemoglobin in red blood cells (RBC) and consequently, microcytic, hypochromic anemia with varying degrees of severity. The disease is a result of mut...

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Dettagli Bibliografici
Pubblicato in:Ann Transl Med
Autori principali: Silao, Catherine Lynn T., Fabella, Terence Diane F., Naranjo, Maria Liza T., Padilla, Carmencita D., Yuson, Ernesto D. J.
Natura: Artigo
Lingua:Inglês
Pubblicazione: AME Publishing Company 2017
Soggetti:
Molecular Genetics, Genomics, Mechanisms of Diseases
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5641812/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s089
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