首页> 外文OA文献 >Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene

【2h】

Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene

机译：II型Crigler-Najjar综合征是由胆红素尿苷5'-二磷酸-葡萄糖醛酸转移酶（UGT1A1）基因的三个不同突变引起的

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
引文网络
相似文献
相关主题

著录项

作者
IOLASCON, A.; MELONI, A.; COPPOLA, B.; ROSATELLI, M. C.;
展开▼
作者单位

展开▼
年度 2000
总页数
原文格式 PDF
正文语种 en
中图分类

相似文献

外文文献
中文文献
专利

1. Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis [J] . Bixia Zheng, Guorui Hu, Jin Yu, BMC Pediatrics . 2014,第1期

机译：一名中国男孩的Crigler-Najjar综合征II型，归因于胆红素尿苷5'-二磷酸-葡萄糖尿苷转移酶（UGT1A1）基因的三个突变和家庭遗传分析
2. A New Type of Defect in the Gene for Bilirubin Uridine 5 '-Diphosphate-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type I [J] . Sachiko Aono, Yasukazu Yamada, Hiroomi Keino, Pediatric Research . 1994,第6期

机译：I型Crigler-Najjar综合征患者胆红素尿苷5'-二磷酸-葡萄糖醛酸转移酶基因的新型缺陷
3. Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II [J] . Kazuo Yamamoto, Hiroshi Sato, Yoshihide Fujiyama, Biochimica et biophysica acta. Molecular basis of disease: BBA . 1998,第3期

机译：胆红素UDP糖基转移酶（UGT1A1）基因的两个错义突变（G71R和Y486D）对吉尔伯特综合征和Crigler-Najjar综合征II型的表型的贡献
4. UGT1A1 gene mutation and hyperthyroidism combined with hepatic failure: case report and literature review [C] . Qianyu Yan, Jingyun Fu International Conference on Biological Information and Biomedical Engineering . 2019

机译：UGT1A1基因突变和甲状腺功能亢进结合肝衰竭：案例报告和文献综述
5. Gain-of-function mutations in SCN5A gene lead to type-3 long QT syndrome [D] . Fang, Fang 2012

机译：SCN5A基因的功能获得性突变导致3型长QT综合征
6. Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis [O] . Bixia Zheng, Guorui Hu, Jin Yu, 2014

机译：一名中国男孩的Crigler-Najjar综合征II型归因于胆红素尿苷5-二磷酸-葡萄糖醛酸转移酶（UGT1A1）基因的三个突变和家庭遗传分析
7. Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis [O] . Bixia Zheng, Guorui Hu, Jin Yu, 2014

机译：一名中国男孩的Crigler-Najjar综合征II型，归因于胆红素尿苷5'-二磷酸-葡萄糖尿苷转移酶（UGT1A1）基因的三个突变和家庭遗传分析

Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene

著录项

引文网络

相似文献

相关主题

期刊订阅