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Mutation of EpCAM leads to intestinal barrier and ion transport dysfunction
ABSTRACT: Congenital tufting enteropathy (CTE) is a devastating diarrheal disease seen in infancy that is typically associated with villous changes and the appearance of epithelial tufts. We previously found mutations in epithelial cell adhesion molecule (EpCAM) to be causative in CTE. We developed...
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| Veröffentlicht in: | J Mol Med (Berl) |
|---|---|
| Hauptverfasser: | , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Springer Berlin Heidelberg
2014
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4408367/ https://ncbi.nlm.nih.gov/pubmed/25482158 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00109-014-1239-x |
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