Associated Papers
Ethnic Variation in G6PD Deficiency: Epidemiology and Mutation Spectrum in Southern China's Multiethnic Hub, Nanning.
Yang J et al.
Clinical Genetics, 2026
Resolving haplotypes of the glucose-6-phosphate dehydrogenase gene using long-range polymerase chain reaction and Oxford Nanopore sequencing.
Chamchoy K et al.
Biology Methods & Protocols, 2026
Two Variants of the ANK1 Gene Associated with Hereditary Spherocytosis.
Bogusławska DM et al.
Biomedicines, 2025
40002721 (PubMed )
Supplement: biomedicines-13-00308-s001.zip › biomedicines-3431635_Additional_file_2-xml.xlsx › AM_enzymopaties
Evaluating the relationship between Clinical G6PD enzyme activity and gene variants.
Zhou X et al.
Peerj, 2024
Epidemiology, evolutionary origin, and malaria-induced positive selection effects of G6PD-deficient alleles in Chinese populations.
Zheng Y et al.
Molecular Genetics & Genomic Medicine, 2020
Incidence of Glucose-6-Phosphate Dehydrogenase Deficiency among Swedish Newborn Infants.
Ohlsson A et al.
International Journal of Neonatal Screening, 2019
Possible association of 3' UTR +357 A>G, IVS11-nt 93 T>C, c.1311 C>T polymorphism with G6PD deficiency.
Sirdah MM et al.
Hematology (amsterdam, Netherlands), 2017
A novel G473A mutation in the glucose-6-phosphate dehydrogenase gene.
Chen X et al.
Pediatric Blood & Cancer, 2010
Molecular and biochemical data on some glucose-6-phosphate dehydrogenase variants from southern Sardinia.
Frigerio R et al.
Haematologica, 0
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