Associated Papers
Rapid detection of G6PD deficiency SNPs using a novel amplicon-based minion sequencing assay.
Tacoli C et al.
Scientific Reports, 2025
41423656 (PubMed )
Supplement: 41598_2025_31822_MOESM3_ESM.xlsx › Sheet1
Rapid detection of G6PD deficiency SNPs using a novel amplicon-based MinION Sequencing Assay.
Tacoli C et al.
Biorxiv : the Preprint Server for Biology, 2025
40666837 (PubMed )
Supplement: media-2.xlsx › Sheet1
Functional interpretation, cataloging, and analysis of 1,341 glucose-6-phosphate dehydrogenase variants.
Geck RC et al.
American Journal of Human Genetics, 2023
36681081 (PubMed )
Supplement: mmc1.xlsx › Table_S1_variants
Severe neonatal jaundice due to a de novo glucose-6-phosphate dehydrogenase deficient mutation.
Del Orbe Barreto R et al.
International Journal of Laboratory Hematology, 2016
Neonatal cholestasis and glucose-6-P-dehydrogenase deficiency.
Kordes U et al.
Pediatric Blood & Cancer, 2010
Molecular analysis of three novel G6PD variants: G6PD Pedoplis-Ckaro, G6PD Piotrkow and G6PD Krakow.
Maciag M et al.
Acta Biochimica Polonica, 2007
A new glucose-6-phosphate dehydrogenase variant G6PD Sugao (826C-->T) exhibiting chronic hemolytic anemia with episodes of hemolytic crisis immediately after birth.
Taki M et al.
International Journal of Hematology, 2001
Hemolytic crisis after excessive ingestion of fava beans in a male infant with G6PD Canton.
Shibuya A et al.
International Journal of Hematology, 1999
Select a paper to view details