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©The Author(s) 2023.
World J Clin Cases. Apr 16, 2023; 11(11): 2443-2451
Published online Apr 16, 2023. doi: 10.12998/wjcc.v11.i11.2443
Published online Apr 16, 2023. doi: 10.12998/wjcc.v11.i11.2443
Table 2 UGT1A1*6 variant combination with glucose-6-phosphate dehydrogenase deficiency in 94 cases of severe neonatal hyperbilirubinemia
| G6PD deficiency | G6PD normal | Total | P value | |
| G211A variation | ||||
| Wild type | 16 | 32 | 48 | 0.787 |
| c.211 hetereozygote | 14 | 23 | 37 | |
| c.211 homozygote | 4 | 5 | 9 | |
| Total | 34 | 60 | 94 |
- Citation: Xu JX, Lin F, Wu YH, Chen ZK, Ma YB, Yang LY. Etiology analysis for term newborns with severe hyperbilirubinemia in eastern Guangdong of China. World J Clin Cases 2023; 11(11): 2443-2451
- URL: https://www.wjgnet.com/2307-8960/full/v11/i11/2443.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v11.i11.2443