Clinical features and genetic variations of severe neonatal hyperbilirubinemia: Five case reports

doi:10.12998/wjcc.v10.i20.6999

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World Journal of Clinical Cases

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Jul 16, 2022; 10(20): 6999-7005
Published online Jul 16, 2022. doi: 10.12998/wjcc.v10.i20.6999

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Figure 1 Polymerase chain reaction-Sanger sequencing results. The mutation sites are indicated by yellow bands. A: SPTB-rs144668591/c.1729A>G heterozygote; B: UGT1A1-rs4148323/c.211G>A heterozygote; C: ABCC2-rs554976086/c.3825C>G heterozygote; D: EPB41-rs188648724/c.1213-4T>G heterozygote; E: EPB41-rs201231112/c.520G>A heterozygote; F: EPB41-rs778090351/c.1474A>G heterozygote.

Citation: Lin F, Xu JX, Wu YH, Ma YB, Yang LY. Clinical features and genetic variations of severe neonatal hyperbilirubinemia: Five case reports. World J Clin Cases 2022; 10(20): 6999-7005
URL: https://www.wjgnet.com/2307-8960/full/v10/i20/6999.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i20.6999