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

A Novel Mutation of ABCB4 in Progressive Familial Intrahepatic Cholestasis 3: Like Mother, Like Daughter.

Journal of clinical gastroenterology - 1 Apr 2016

Wang Zhaoyue, Yang Fan, Wang Jianshe, Ma Xiong

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 ATP Binding Cassette Transporter, Subfamily B
Share to Cholestasis, Intrahepatic
Share to DNA Mutational Analysis
Share to Heredity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Liver Function Tests

Share to Liver Transplantation

Share to Mothers

Share to Treatment Outcome

Source

Identifiers

PMID: 26796082
DOI: 10.1097/MCG.0000000000000474

Genes

ABCB4

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

A Novel Mutation of ABCB4 in Progressive Familial Intrahepatic Cholestasis 3: Like Mother, Like Daughter.PMID 26796082Read ↗

ABCB4 Gene Aberrations in Human Liver Disease: An Evolving SpectrumSemantic proximity Read ↗

Two novel mutations in African and Asian children with progressive familial intrahepatic cholestasis type 3.Semantic proximity Read ↗

[Clinical phenotype and genotype analysis of progressive familial intrahepatic cholestasis type 3 caused by novel ABCB4 gene mutation].Semantic proximity Read ↗

Case Report: A rare case of young adult progressive familial intrahepatic cholestasis-type 3 with a novel heterozygous pathogenic variant of ABCB4Semantic proximity Read ↗

A case of progressive familial intrahepatic cholestasis type 1 with compound heterozygous mutations of ATP8B1.Semantic proximity Read ↗

ABCB4 disease: Many faces of one gene deficiency.Semantic proximity Read ↗

A Novel Variant (p.Leu1054Arg) in ABCB11 Presenting with Progressive Familial Intrahepatic Cholestasis (PFIC) with Congenital Hypothyroidism.Semantic proximity Read ↗

[Clinical and genetic analysis of cases of progressive familial intrahepatic cholestasis type 3].Semantic proximity Read ↗

Novel ABCB4 mutation in a Chinese female patient with progressive familial intrahepatic cholestasis type 3: a case report.Semantic proximity Read ↗

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

Type 3 of progressive familial intrahepatic cholestasis (PFIC-3): Case reportSemantic proximity Read ↗

A female of progressive familial intrahepatic cholestasis type 3 caused by heterozygous mutations of ABCB4 gene and her cirrhosis improved after treatment of ursodeoxycholic acid: a case report.Semantic proximity Read ↗

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