Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Chinese
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Role of glucose phosphate deficiency in neonatal hyperbilirubinemia among local population of Pakistan;Pakistan BioMedical Journal;2022-03-01
2. Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong;BMC Pediatrics;2021-12
3. Level of apoptosis in Saudi patients with a defect in Glucose-6-phosphate dehydrogenase (G6PD);Journal of King Saud University - Science;2021-09
4. Prevalence and molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Lue ethnic group of northern Thailand;Scientific Reports;2021-02-03
5. Genetic Factors and Delayed TSB Monitoring and Treatment as Risk Factors Associated with Severe Hyperbilirubinemia in Term Neonates Admitted for Phototherapy;Journal of Tropical Pediatrics;2020-06-24
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