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Distribution of G6PD deficiency genotypes among Southeast Asian populations

20 Dec 2021

Abstract excerpt

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a group of X-linked, hereditary genetic disorders caused by mutations in the G6PD gene and results in functional variants of about 400 biochemical and clinical phenotypes. Among them, more than 215 genotypes have been identified so far. In this review, specific features of the genotype distribution in different communities and countries are discussed based on...

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PMID: 34930507
DOI: 10.1186/s41182-021-00387-z

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