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Article

XIAP variants in male Crohn's disease.

Gut - 1 Jan 2015

Zeissig Yvonne, Petersen Britt-Sabina, Milutinovic Snezana, Bosse Esther, Mayr Gabriele, Peuker Kenneth, Hartwig Jelka, Keller Andreas, Kohl Martina, Laass Martin W, Billmann-Born Susanne, Brandau Heide, Feller Alfred C, Röcken Christoph, Schrappe Martin, Rosenstiel Philip, Reed John C, Schreiber Stefan, Franke Andre, Zeissig Sebastian

Abstract excerpt

OBJECTIVE: The genetic basis of inflammatory bowel disease (IBD) is incompletely understood. The aim of this study was to identify rare genetic variants involved in the pathogenesis of IBD. DESIGN: Exome sequencing and immunological profiling were performed in a patient with early onset Crohn's disease (CD). The coding region of the gene encoding X-linked inhibitor of apoptosis protein (XIAP) was sequenced in...

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Source

Identifiers

PMID: 24572142
DOI: 10.1136/gutjnl-2013-306520

Genes

XIAP
NOD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

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XIAP variants in male Crohn's disease.PMID 24572142Read ↗

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Analysis of Genes Associated With Monogenic Primary Immunodeficiency Identifies Rare Variants in XIAP in Patients With Crohn’s DiseaseSemantic proximity Read ↗

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