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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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| Publicado no: | Anemia |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7886513/ https://ncbi.nlm.nih.gov/pubmed/33628497 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2021/6680925 |
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