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: Boonchai Boonyawat Tim Phetthong Nithipun Suksumek Chanchai Traivaree Source Type: research
More News: Anemia | Children | G6PD | Genetics | Hematology | Pediatrics | Perinatology & Neonatology | Study | Thailand Health