Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification

α-Thalassaemia is an inherited haemoglobin disorder that results from the defective synthesis of α-globin protein. Couples whom both carry the α-thalassaemia 1 gene are at risk of having a foetus with the most severe thalassaemia, Hb Bart’s hydrops fetalis, with a risk of maternal mortality. However...

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Detalles Bibliográficos
Autores principales: Chumworathayee, Worakawee, Munkongdee, Thongperm, Buasuwan, Nattrika, Chaichompoo, Pornthip, Svasti, Saovaros
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10264369/
https://www.ncbi.nlm.nih.gov/pubmed/37311778
http://dx.doi.org/10.1038/s41598-023-36676-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10264369/
https://www.ncbi.nlm.nih.gov/pubmed/37311778
http://dx.doi.org/10.1038/s41598-023-36676-2

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