Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong

被引：0
作者：
Jia-Xin Xu
Fen Lin
Zi-Kai Chen
Zhao-Yun Luo
Xiao-Fen Zhan
Jiao-Ren Wu
Yu-Bin Ma
Jian-Dong Li
Li-Ye Yang
机构：
[1] Chaozhou Central Hospital Affiliated to Southern Medical University,Central Laboratory
[2] Hanshan Normal University,School of Food Engineering and Biotechnology
[3] Chaozhou Central Hospital Affiliated to Southern Medical University,Department of Pediatrics
[4] People’s Hospital of Yangjiang Affiliated to Guangdong Medical University,Precision Medical Center
来源：
BMC Pediatrics | / 21卷
关键词：
Neonatal hyperbilirubinemia; Glucose-6-phosphate dehydrogenase deficiency; Uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1);
D O I：
暂无
中图分类号：
学科分类号：
摘要：
引用
收藏
相关论文
共 112 条
  • [1] Stocker R(1987)Bilirubin is an antioxidant of possible physiological importance Science. 235 1043-1046
  • [2] Yamamoto Y(1974)Measurement of red blood cell life-span JAMA 230 1304-1305
  • [3] Mcdonagh AF(2001)Neonatal Hyperbilirubinemia N Engl J Med 344 581-590
  • [4] Glazer AN(2012)Glucose-6-phosphate dehydrogenase, NADPH, and cell survival IUBMB Life 64 362-369
  • [5] Ames BN(2008)Glucose-6-phosphate dehydrogenase deficiency Lancet. 371 64-74
  • [6] Brouillard RP(2009)The global prevalence of glucose-6-phosphate dehydrogenase deficiency: a systematic review and meta-analysis Blood Cells Mol Dis 42 267-278
  • [7] Dennery PA(2016)Glucose-6-phosphate dehydrogenase deficiency Hematol Oncol Clin North Am 30 373-393
  • [8] Seidman DS(2016)Glucose-6-phosphate dehydrogenase: update and analysis of new mutations around the world Int J Mol Sci 17 2069-311
  • [9] Stevenson DK(2010)Rapid and reliable detection of glucose-6-phosphate dehydrogenase (G6PD) gene mutations in Han Chinese using high-resolution melting analysis J Mol Diagn 12 305-336
  • [10] Stanton RC(2017)Association between UridinDiphosphateGlucuronosylotransferase 1A1(UGT1A1) gene polymorphism and neonatal Hyperbilirubinemia ActaBiochim Pol 64 351-26
12345678910