UGT1A1*6 mutation associated with the occurrence and severity in infants with prolonged jaundice

BACKGROUND: This study aimed to investigate the influence of a variant of the UGT1A1 gene on the occurrence and severity of prolonged jaundice in Chinese infants at term. METHODS: 175 infants with prolonged jaundice and 149 controls were used in this retrospective case-control study. The infants wit...

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Detalles Bibliográficos
Autores principales: Yang, Zhe, Lin, Fen, Xu, Jia-Xin, Yang, Hui, Wu, Yong-Hao, Chen, Zi-Kai, Xie, He, Huang, Bin, Lin, Wei-Hao, Wu, Jian-Peng, Ma, Yu-Bin, Li, Jian-Dong, Yang, Li-Ye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808393/
https://www.ncbi.nlm.nih.gov/pubmed/36605758
http://dx.doi.org/10.3389/fped.2022.1080212

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808393/
https://www.ncbi.nlm.nih.gov/pubmed/36605758
http://dx.doi.org/10.3389/fped.2022.1080212

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