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Dysregulations of lysosomal storage, mitochondrial function, peroxisomes, cytoskeleton function and related crosstalk described in microgravity or following exposure to GCR are also the main determinants of several inherited metabolic disorders in newborns

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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