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

Background. Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common X-linked inherited erythroenzymopathy in Thailand. The clinical and hematological manifestations of G6PD deficiency are variable. Objective. This study aimed to characterize the genotype-phenotype correlation of G6PD...

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Bibliographic Details
Main Authors: Boonchai Boonyawat, Tim Phetthong, Nithipun Suksumek, Chanchai Traivaree
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Anemia
Online Access:http://dx.doi.org/10.1155/2021/6680925
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