Crigler Najjar Syndrome, Type 1
Last Posted: May 12, 2023
- [A family study of the compound heterozygous mutation of the UGT1A1 gene causing Crigler-Najjar syndrome type II].
L Luo, et al. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2023 0 (2) 168-173
- Bilirubin metabolism and UDP-glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response.
Huang May-Jen, et al. The Kaohsiung journal of medical sciences 2022 0 (8) 729-738
- Gilbert Syndrome and Genetic Findings in Children: A Tertiary-Center Experience from Turkey.
Ça?an Appak Yeliz, et al. Turkish archives of pediatrics 2022 0 (3) 295-299
- Gilbert or Crigler-Najjar syndrome? Neonatal severe unconjugated hyperbilirubinemia with P364L UGT1A1 homozygosity.
Cozzi Laura, et al. Italian journal of pediatrics 2022 0 (1) 59
- [Study on spectrum of UGT1A1 mutations in connection with inherited non-hemolytic unconjugated hyperbilirubinemia].
Xiong Q F, et al. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2019 0 (12) 898-902
- Novel combined UGT1A1 mutations in Crigler Najjar Syndrome type I.
Abdellaoui Nawel, et al. Journal of clinical laboratory analysis 2022 6 (6) e24482
- UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlation.
Abuduxikuer Kuerbanjiang, et al. Medicine 2018 12 (49) e13576
- Spectrum of UGT1A1 Variations in Chinese Patients with Crigler-Najjar Syndrome Type II.
Li Lufeng, et al. PloS one 2015 0 (5) e0126263
- [Mutation analysis of UGT1A1 gene in patients with unconjugated hyperbilirubinemia].
Sun Shun-chang, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2013 8 (4) 425-8
- Crigler Najjar syndrome, type 1
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