Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan.
Yi-Hao WengYa-Wen ChiuShao-Wen ChengChun-Yuh YangPublished in: BMC pediatrics (2016)
G6PD deficiency, short HO-1 promoter GT-repeat and GA at nt211 in UGT1A1 are risk factors of neonatal hyperbilirubinemia. The data provide clinical evidence to explain the high incidence of neonatal hyperbilirubinemia in Taiwan.