Glucose-6-phosphate dehydrogenase deficiency and neonatal hyperbilirubinemia: insights on pathophysiology, diagnosis, and gene variants in disease heterogeneity

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  • who: Fook Choe Cheah from the Department of Paediatrics, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Cheras, Malaysia, CNC-Centre for Neuroscience Cell Biology, University of Coimbra, Coimbra, Portugal, Coimbra Chemistry have published the article: Glucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia: Insights on Pathophysiology, Diagnosis, and Gene Variants in Disease Heterogeneity, in the Journal: (JOURNAL)
  • future: More research is needed to study the role of Prdx2 in jaundiced G6PDdeficient infants with and without acute hemolysis. Such investigative approaches not only help to accelerate discovery of novel variants for diagnosis but also aid . . .

     

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