UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice.
Yang Z, Lin F, Xu JX, Yang H, Wu YH, Chen ZK, Xie H, Huang B, Lin WH, Wu JP, Ma YB, Li JD, Yang LY.
Yang Z, et al. Among authors: li jd.
Front Pediatr. 2022 Dec 20;10:1080212. doi: 10.3389/fped.2022.1080212. eCollection 2022.
Front Pediatr. 2022.
PMID: 36605758
Free PMC article.