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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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| Veröffentlicht in: | J Clin Transl Hepatol |
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| Hauptverfasser: | , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
XIA & HE Publishing Inc.
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8111108/ https://ncbi.nlm.nih.gov/pubmed/34007799 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14218/JCTH.2020.00108 |
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