Distribution of G6PD deficiency genotypes among Southeast Asian populations

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...

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Detalles Bibliográficos
Autores principales: Tantular, Indah S., Kawamoto, Fumihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686385/
https://www.ncbi.nlm.nih.gov/pubmed/34930507
http://dx.doi.org/10.1186/s41182-021-00387-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8686385/
https://www.ncbi.nlm.nih.gov/pubmed/34930507
http://dx.doi.org/10.1186/s41182-021-00387-z

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