Characterization of G6PD genotypes and phenotypes on the northwestern
Mutations in the glucose-6-phosphate dehydrogenase (G6PD) gene result in red blood cells with increased susceptibility to oxidative damage. Significant haemolysis can be caused by primaquine and other 8-aminoquinoline antimalarials used for the radical treatment of Plasmodium vivax malaria. The dist...
Main Authors: | Bancone, G, Chu, C, Somsakchaicharoen, R, Chowwiwat, N, Parker, D, Charunwatthana, P, White, N, Nosten, F |
---|---|
Formato: | Journal article |
Idioma: | English |
Publicado: |
Public Library of Science
2014
|
Títulos similares
-
Characterization of G6PD Genotypes and Phenotypes on the Northwestern Thailand-Myanmar Border
por: Bancone, G, et al.
Publicado: (2014) -
Characterization of G6PD genotypes and phenotypes on the northwestern Thailand-Myanmar border.
por: Germana Bancone, et al.
Publicado: (2014-01-01) -
Cytochemical flow analysis of intracellular G6PD and aggregate analysis of mosaic G6PD expression.
por: Kalnoky, M, et al.
Publicado: (2017) -
The G6PD flow-cytometric assay is a reliable tool for diagnosis of G6PD deficiency in women and anaemic subjects
por: Bancone, G, et al.
Publicado: (2017) -
Primaquine-induced haemolysis in females heterozygous for G6PD deficiency
por: Chu, C, et al.
Publicado: (2018)