Rapid molecular diagnostics of large deletional β(0)-thalassemia (3.5 kb and 45 kb) using colorimetric LAMP in various thalassemia genotypes

BACKGROUND: β-thalassemia is an inherited disorder that is reported worldwide. Two common β(0)-thalassemia mutations (3.5 kb and 45 kb deletions) are prevalent in Southeast Asia and Thailand. Identification of these defects is essential to population screening and prenatal diagnosis. We aimed to dev...

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Detalles Bibliográficos
Autores principales: Tepakhan, Wanicha, Jomoui, Wittaya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591500/
https://www.ncbi.nlm.nih.gov/pubmed/34816050
http://dx.doi.org/10.1016/j.heliyon.2021.e08372

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591500/
https://www.ncbi.nlm.nih.gov/pubmed/34816050
http://dx.doi.org/10.1016/j.heliyon.2021.e08372

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