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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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Detalles Bibliográficos
Autores principales:	Boonyawat, Boonchai, Phetthong, Tim, Suksumek, Nithipun, Traivaree, Chanchai
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2021
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7886513/ https://www.ncbi.nlm.nih.gov/pubmed/33628497 http://dx.doi.org/10.1155/2021/6680925

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