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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Anemia
Päätekijät: Boonyawat, Boonchai, Phetthong, Tim, Suksumek, Nithipun, Traivaree, Chanchai
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Hindawi 2021
Aiheet:
Research Article
Linkit: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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