Ugt1a1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice

HIGHLIGHTS

• who: Zhe Yang et al. from the Clinical data and specimen collection This retrospective case-control study was carried out at Chaozhou Central Hospital affiliated to Southern Medical University, ChinaIn-hospital neonates from Department of Neonatology or General Pediatrics from February , to November , were selected have published the research: UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice, in the Journal: (JOURNAL)
• what: This study aimed to explore the contribution of the UGT1A1*6 variant to prolonged jaundice in term infants of Chinese ancestry. The authors also assessed multiple risk . . .
  

   

  

  If you want to have access to all the content you need to log in!

  Thanks :)

  Username or Email

  Password

  Remember me

  Lost your password?

  If you don't have an account, you can create one here.