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Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia

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Ein Mangel kann sich schleichend durch chronische Erschpfung, anhaltende Mdigkeit und eine sprbar verlangsamte Regeneration nach sportlicher oder geistiger Anstrengung zeigen [8]

Two homologous NRP isoforms are known to exist, namely NRP1 and NRP2, encoded by distinct neuropilin genes ( Nrp1 and Nrp2 ) 315,316,317

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1d and Supplementary Tables 813) and used those together with karyotyping, clinical covariates and central histopathological review to classify AML according to the established ELN 2 and 2024 WHO 9 classifications