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