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

Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11

1 Aug 2004

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 Drug Transport and Resistance Mechanisms
Share to Liver Diseases and Immunity
Share to Pediatric Hepatobiliary Diseases and Treatments

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15300568
DOI: 10.1053/j.gastro.2004.04.065

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11PMID 15300568Read ↗

Compound heterozygous mutations of ABCB11 responsible for benign recurrent intrahepatic cholestasis.Semantic proximity Read ↗

Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy.Semantic proximity Read ↗

Update on progressive familial intrahepatic cholestasis.Semantic proximity Read ↗

New Insights in Genetic Cholestasis: From Molecular Mechanisms to Clinical ImplicationsSemantic proximity Read ↗

ATP8B1, ABCB11, and ABCB4 Genes Defects: Novel Mutations Associated with Cholestasis with Different Phenotypes and Outcomes.Semantic proximity Read ↗

A Rare Case of Benign Recurrent Intrahepatic Cholestasis Initially Diagnosed in Middle-age.Semantic proximity Read ↗

Description of two new ABCB11 mutations responsible for type 2 benign recurrent intrahepatic cholestasis in a French-Canadian family.Semantic proximity Read ↗

Variations of ABCB4 and ABCB11 genes are associated with primary intrahepatic stones.Semantic proximity Read ↗

A Comprehensive Review of Progressive Familial Intrahepatic Cholestasis (PFIC): Genetic Disorders of Hepatocanalicular TransportersSemantic proximity Read ↗

Clinical and genetic characterization of pediatric patients with progressive familial intrahepatic cholestasis type 3 (PFIC3): identification of 14 novel ABCB4 variants and review of the literaturesSemantic proximity Read ↗

Heterozygous mutations of ATP8B1, ABCB11 and ABCB4 cause mild forms of Progressive Familial Intrahepatic Cholestasis in a pediatric cohort.Semantic proximity Read ↗

Cholestatic liver disease.Semantic proximity Read ↗

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