Loss of Syntaxin 3 Causes Variant Microvillus Inclusion Disease-Reference-Cited by-同舟云学术

Loss of Syntaxin 3 Causes Variant Microvillus Inclusion Disease

Published:2014-07 Issue:1 Volume:147 Page:65-68.e10
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Wiegerinck Caroline L.,Janecke Andreas R.,Schneeberger Kerstin,Vogel Georg F.,van Haaften–Visser Désirée Y.,Escher Johanna C.,Adam Rüdiger,Thöni Cornelia E.,Pfaller Kristian,Jordan Alexander J.,Weis Cleo–Aron,Nijman Isaac J.,Monroe Glen R.,van Hasselt Peter M.,Cutz Ernest,Klumperman Judith,Clevers Hans,Nieuwenhuis Edward E.S.,Houwen Roderick H.J.,van Haaften Gijs,Hess Michael W.,Huber Lukas A.,Stapelbroek Janneke M.,Müller Thomas,Middendorp Sabine

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference21 articles.

1. Microvillous inclusion disease (microvillous atrophy)

2. Neonatal Enteropathies: Defining the Causes of Protracted Diarrhea of Infancy

3. Microvillous Inclusion Disease: An Evolving Condition

4. Microvillous Inclusion Disease: Ultrastructural Variability

5. MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity

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