Single-Drop Blood Detection of Common G6PD Mutations in Thailand Based on Allele-Specific Recombinase Polymerase Amplification with CRISPR-Cas12a

[Image: see text] Glucose 6-phosphate dehydrogenase (G6PD) deficiency is the most common inherited enzymopathy. Identification of the G6PD deficiency through screening is crucial to preventing adverse effects associated with hemolytic anemia following antimalarial drug exposure. Therefore, a rapid a...

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Detalles Bibliográficos
Autores principales: Mungkalasut, Punchalee, Nimsamer, Pattaraporn, Cheepsunthorn, Poonlarp, Payungporn, Sunchai, Cheepsunthorn, Chalisa Louicharoen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10688097/
https://www.ncbi.nlm.nih.gov/pubmed/38046356
http://dx.doi.org/10.1021/acsomega.3c05596

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10688097/
https://www.ncbi.nlm.nih.gov/pubmed/38046356
http://dx.doi.org/10.1021/acsomega.3c05596

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