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Association Between udp-glucuronosyltransferase 1a1 (ugt1a1) Gene Polymorphism, (c.-3279t>g) and Phototherapy among Glucose-6-Phosphate Dehydrogenase (g6pd)-Deficient Neonates

Author

Listed:
  • Fook-Choe Cheah
  • Fei-Liang Wong

    (Department of Pediatrics, Universiti Kebangsaan Malaysia Medical Centre, Malaysia)

  • Azlin Ithnin

    (Department of Pathology, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Malaysia)

  • Ainoon Othman

    (Department of Pathology, Faculty of Medicine, Universiti Sains Islam Malaysia, Malaysia)

Abstract

Hyperbilirubinemia is one of the most commonly encountered conditions even in otherwise healthy newborn infants in the first week of life...

Suggested Citation

  • Fook-Choe Cheah & Fei-Liang Wong & Azlin Ithnin & Ainoon Othman, 2018. "Association Between udp-glucuronosyltransferase 1a1 (ugt1a1) Gene Polymorphism, (c.-3279t>g) and Phototherapy among Glucose-6-Phosphate Dehydrogenase (g6pd)-Deficient Neonates," Biomedical Journal of Scientific & Technical Research, Biomedical Research Network+, LLC, vol. 2(1), pages 2451-2453, January.
    • Handle: RePEc:abf:journl:v:2:y:2018:i:1:p:2451-2453
    DOI: 10.26717/BJSTR.2018.2.000714
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