PMID 3393536 1988 Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.
PMID 8611726 1996 Multiple G6PD mutations are associated with a clinical and biochemical phenotype similar to that of G6PD Mediterranean.
PMID 24460025 2014 Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency in Greek newborns: the Mediterranean C563T mutation screening.
PMID 23479361 2013 Glucose-6-phosphate dehydrogenase deficient variants are associated with reduced susceptibility to malaria in the Brazilian Amazon.
PMID 19594365 2009 G6PD Mediterranean S188F codon mutation is common among Saudi sickle cell patients and increases the risk of stroke.
PMID 22906047 2012 Neonatal hyperbilirubinemia in infants with G6PD c.563C > T Variant.
PMID 1978555 1990 Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East.
PMID 15315792 2005 Molecular basis of G6PD deficiency in India.
PMID 15502081 2004 In silico prediction of the deleterious effect of a mutation: proceed with caution in clinical genetics.
rs5030868 in
G6PD gene and
Hemoglobin A measurement
PMID 26366553 2015 Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.
rs5030868 in
G6PD gene and
Hemoglobin measurement
PMID 26366553 2015 Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.
rs5030868 in
G6PD gene and
MALARIA, SUSCEPTIBILITY TO (finding)
PMID 19594365 2009 G6PD Mediterranean S188F codon mutation is common among Saudi sickle cell patients and increases the risk of stroke.
PMID 24586352 2014 A population survey of the glucose-6-phosphate dehydrogenase (G6PD) 563C>T (Mediterranean) mutation in Afghanistan.
PMID 3393536 1988 Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.
PMID 23479361 2013 Glucose-6-phosphate dehydrogenase deficient variants are associated with reduced susceptibility to malaria in the Brazilian Amazon.
PMID 22906047 2012 Neonatal hyperbilirubinemia in infants with G6PD c.563C > T Variant.