UGT1A1-related Bilirubin Encephalopathy/Kernicterus in Adults

BACKGROUND AND AIMS: Bilirubin encephalopathy/kernicterus is very rare in adults. This study is aimed to investigate the clinical manifestations and genetic features of two patients with UGT1A1-related kernicterus. METHODS: Sanger sequencing analysis was performed to identify UGT1A1 gene mutations i...

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Detalles Bibliográficos
Autores principales: Bai, Jie, Li, Lu, Liu, Hui, Liu, Shuang, Bai, Li, Song, Wenyan, Chen, Yu, Zheng, Sujun, Duan, Zhongping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: XIA & HE Publishing Inc. 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111108/
https://www.ncbi.nlm.nih.gov/pubmed/34007799
http://dx.doi.org/10.14218/JCTH.2020.00108

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111108/
https://www.ncbi.nlm.nih.gov/pubmed/34007799
http://dx.doi.org/10.14218/JCTH.2020.00108

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