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Article

A Novel Compound-Heterozygous Epithelial Cell Adhesion Molecule Mutation in Tufting Enteropathy.

Journal of pediatric gastroenterology and nutrition - 1 Jan 2017

Shakhnovich Valentina, Dinwiddie Darrell, Hildreth Amber, Attard Thomas, Kingsmore Stephen

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Share to Diarrhea, Infantile
Share to Epithelial Cell Adhesion Molecule
Share to Infant
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 25383784
DOI: 10.1097/MPG.0000000000000629
PMCID: PMC4426084

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Related research

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A Novel Compound-Heterozygous Epithelial Cell Adhesion Molecule Mutation in Tufting Enteropathy.PMID 25383784Read ↗

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Case Series of Eight Congenital Tufting Enteropathy Patients and Literature Review.Semantic proximity Read ↗

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Novel CD55 Mutation Associated With Severe Small Bowel Ulceration Mimicking Inflammatory Bowel Disease in a Pair of Siblings.Semantic proximity Read ↗

Novel Mutations in EPCAM Cause Congenital Tufting Enteropathy.Semantic proximity Read ↗

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Further evidence for EpCAM as the gene for congenital tufting enteropathy.Semantic proximity Read ↗

Mutation of EpCAM leads to intestinal barrier and ion transport dysfunction.Semantic proximity Read ↗

EPCAMmutation update: Variants associated with congenital tufting enteropathy and Lynch syndromeSemantic proximity Read ↗

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