Molecular Analysis of theUGT1A1Gene in Korean Patients with Crigler-Najjar Syndrome Type II-Reference-Cited by-同舟云学术

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Molecular Analysis of theUGT1A1Gene in Korean Patients with Crigler-Najjar Syndrome Type II

Published:2014 Issue:1 Volume:17 Page:37
ISSN:2234-8646
Container-title:Pediatric Gastroenterology, Hepatology & Nutrition
language:en
Short-container-title:Pediatr Gastroenterol Hepatol Nutr

Author:

Ko Jae Sung¹,Chang Ju Young¹,Moon Jin Soo¹,Yang Hye Ran¹,Seo Jeong Kee¹

Affiliation:

1. Department of Pediatrics, Seoul National University College of Medicine, Seoul, Korea.

Funder

Seoul National University Hospital

Publisher

The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition

Subject

Gastroenterology,Hepatology,Pediatrics, Perinatology, and Child Health

Link

https://synapse.koreamed.org/pdf/10.5223/pghn.2014.17.1.37

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Should We Consider UGT1A1 Mutation Analysis in Evaluating the Prolonged Jaundice of Newborn Infants?;Neonatal Medicine;2024-02-29

2. Effect of the genetic mutant G71R in uridine diphosphate-glucuronosyltransferase 1A1 on the conjugation of bilirubin;Open Life Sciences;2022-01-01

3. Genetic Spectrum ofUGT1A1in Korean Patients with Unconjugated Hyperbilirubinemia;Annals of Laboratory Medicine;2020-05-01

4. Uridine 5'‑diphospho‑glucronosyltrasferase: Its role in pharmacogenomics and human disease (Review);Experimental and Therapeutic Medicine;2018-05-18

5. Correlation between UGT1A1 polymorphism and neonatal hyperbilirubinemia of neonates in Wuhan;Current Medical Science;2017-10

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