Genotype-Phenotype Correlation of G6PD Mutations among Central Thai Children with G6PD Deficiency

CONCLUSION: This study characterizes the molecular heterogeneity of G6PD variants causing G6PD deficiency in Thai children. Our study demonstrated the efficiency of direct DNA sequencing which can identify 12 missense mutations in Thai children.PMID:33628497 | PMC:PMC7886513 | DOI:10.1155/2021/6680925
Source: Anemia - Category: Hematology Authors: Source Type: research