Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[The analysis of UGT1A1 gene mutations in hereditary unconjugated hyperbilirubinemia].

Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology - 20 Nov 2016

Sun L, Zhang L, Li M, Teng X Y, Qi L M, Zhou X G, Lang Z W, Wang P

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Bilirubin
Share to Crigler-Najjar Syndrome
Share to Gilbert Disease
Share to Glucuronosyltransferase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 27978934
DOI: 10.3760/cma.j.issn.1007-3418.2016.11.013
PMCID: PMC12769582

Genes

UGT1A1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[The analysis of UGT1A1 gene mutations in hereditary unconjugated hyperbilirubinemia].PMID 27978934Read ↗

[Prolonged neonatal hyperbilirubinemia associated with a UGT1A1 gene mutation].Semantic proximity Read ↗

Genetic Spectrum of UGT1A1 in Korean Patients with Unconjugated Hyperbilirubinemia.Semantic proximity Read ↗

[Study on spectrum of UGT1A1 mutations in connection with inherited non-hemolytic unconjugated hyperbilirubinemia].Semantic proximity Read ↗

[Correlation between the mutation spectrum of the UGT1A1 gene and clinical phenotype in patients with inherited hyperunconjugated bilirubinemia].Semantic proximity Read ↗

[Progress in the study of UDP-glucuronosyltransferase gene polymorphism].Semantic proximity Read ↗

[Genetic analysis of a child affected with Crigler-Najjar syndrome type II].Semantic proximity Read ↗

Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia.Semantic proximity Read ↗

[UGT1A1 gene mutation spectrum with indirect hyperbilirubinemia in children].Semantic proximity Read ↗

[Roles of UGT 1A1 gene mutation in the development of neonatal hyperbilirubinemia in Guangxi].Semantic proximity Read ↗

UGT1A1 genetic analysis as a diagnostic aid for individuals with unconjugated hyperbilirubinemia.Semantic proximity Read ↗

Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia.Semantic proximity Read ↗

Analysis of uridine diphosphate glucuronosyl transferase 1A1 gene mutations in neonates with unconjugated hyperbilirubinemia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.