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Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization. (2010)

First Author: Cullinane AR

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng.538

PubMed Identifier: 20190753

Publication URI: http://europepmc.org/abstract/MED/20190753

Type: Journal Article/Review

Volume: 42

Parent Publication: Nature genetics

Issue: 4

ISSN: 1061-4036