Lin Y.-J.PO-NIEN TSAO2020-12-222020-12-2220181875-9572https://www.scopus.com/inward/record.uri?eid=2-s2.0-85029470624&doi=10.1016%2fj.pedneo.2017.01.008&partnerID=40&md5=2508c5928e336b9c121b41a4fd3b39e9https://scholars.lib.ntu.edu.tw/handle/123456789/530184[SDGs]SDG3bilirubin; glucuronosyltransferase 1A1; glucuronosyltransferase; artificial milk; Asian; bilirubin blood level; brain damage; brain region; breast feeding; disease severity; genetic variation; glucose 6 phosphate dehydrogenase deficiency; heterozygote; homozygote; Letter; neonatal hyperbilirubinemia; promoter region; risk factor; TATA box; thalassemia; human; newborn; Glucuronosyltransferase; Humans; Hyperbilirubinemia, Neonatal; Infant, Newborn211 G to A variation of UGT1A1 and severe neonatal hyperbilirubinemialetter10.1016/j.pedneo.2017.01.008289275822-s2.0-85029470624