Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II-Reference-Cited by-同舟云学术

Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II

Published:2017-11 Issue:45 Volume:96 Page:e8620
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Sun Lei,Li Man,Zhang Liang,Teng Xiaoying,Chen Xiangmei,Zhou Xingang,Ma Zhiyuan,Qi Liming,Wang Peng

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference27 articles.

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2. Role of a homozygous A(TA)7TAA promoter polymorphism and an exon 1 heterozygous frameshift mutation UGT1A1 in Crigler-Najjar syndrome type II in a Thai neonate;Nilyanimit;Genet Mol Res,2013

3. Inherited disorders of bilirubin transport and conjugation: new insights into molecular mechanisms and consequences;Erlinger;Gastroenterology,2014

4. Gilbert syndrome;Fretzayas;Eur J Pediatr,2012

5. Gilbert's syndrome and the risk of death: a population-based cohort study;Horsfall;J Gastroenterol Hepatol,2013

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