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Summary Keywords molecular screening, bilirubin, favism, hemolytic anemia, neonatal jaundice, peroxiredoxin 2, Heinz bodies, G6PD Citation Lee HY, Ithnin A, Azma RZ, Othman A, Salvador A and Cheah FC (2022) Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity
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A subsequent study by the same authors that examined the association between nonarteritic anterior ischemic optic neuropathy and G6PD deficiency found a barely detectable statistically significant association (univariate, P = 0.02
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