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Molecular Characterization and Genotype-Phenotype Correlation of G6PD Mutations in Five Ethnicities of Northern Vietnam

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme disorder and is caused by G6PD gene mutations. To date, more than 400 variants in the G6PD gene have been discovered, and about 160 identified variants are associated with a significant decrease in the G6PD enzyme activity...

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Detalles Bibliográficos
Autores principales:	Ngo, Thi Thao, Tran, Thinh Huy, Ta, Thanh Dat, Le, Thi Phuong, Nguyen, Phuoc Dung, Tran, Mai Anh, Bui, The-Hung, Ta, Thanh Van, Tran, Van Khanh
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2022
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277213/ https://www.ncbi.nlm.nih.gov/pubmed/35845714 http://dx.doi.org/10.1155/2022/2653089

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