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...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:J Mol Med (Berl)
Päätekijät: Kozan, Philip A., McGeough, Matthew D., Peña, Carla A., Mueller, James L., Barrett, Kim E., Marchelletta, Ronald R., Sivagnanam, Mamata
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Springer Berlin Heidelberg 2014
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Original Article
Linkit: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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