Article

Investigation of the Association Between G6PD, UGT1A1, and SLCO1B1 Gene Polymorphisms and Neonatal Hyperbilirubinemia Using MALDI-TOF MS Technology

2026-06-23

Abstract excerpt

<title>Abstract</title> <p> Objective: To investigate the relationship between <italic>neonatal G6PD deficiency and G6PD, UGT</italic> 1A <italic>1,</italic> and <italic>SLCO1B1</italic> gene polymorphisms and phenotypes, as well as their association with neonatal hyperbilirubinemia (NHB), using MALDI-TOF MS technology. <h4>Methods:</h4> A total of 210 cases of neonatal hyperbilirubinemia were selected as...

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Literature Corpus work: 61d1cc2f-1c1f-5308-9e3a-9fea90eaf58b
DOI: 10.21203/rs.3.rs-9967522/v1

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