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Article

Arthrogryposis, renal dysfunction, and cholestasis syndrome caused by VIPAR mutation.

Journal of pediatric gastroenterology and nutrition - 1 Mar 2014

Ackermann Oanez, Gonzales Emmanuel, Keller Marion, Guettier Catherine, Gissen Paul, Jacquemin Emmanuel

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Share to Arthrogryposis
Share to Carrier Proteins
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 23636179
DOI: 10.1097/MPG.0b013e318298108f

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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Arthrogryposis, renal dysfunction, and cholestasis syndrome caused by VIPAR mutation.PMID 23636179Read ↗

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[Clinical features and VPS33B mutations in a family affected by arthrogryposis, renal dysfunction, and cholestasis syndrome].Semantic proximity Read ↗

Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization.Semantic proximity Read ↗

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