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

Andrew R. Cullinane, Anna Straatman-Iwanowska, Andreas Zaucker, Yoshiyuki Wakabayashi, Christopher K. Bruce, Guanmei Luo, Fatimah Rahman, Figen Gürakan, Eda Utine, Tanju B. Zkan, Jonas Denecke, Jurica Vukovic, Maja Di Rocco, Hanna Mandel, Hakan Cangul, Randolph P. Matthews, Steve G. Thomas, Joshua Z. Rappoport, Irwin M. Arias, Hartwig WolburgA. S. Knisely, Deirdre A. Kelly, Ferenc Müller, Eamonn R. Maher, Paul Gissen*

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

127 Scopus citations

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Medicine & Life Sciences