Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization
Andrew R. Cullinane(University of Birmingham), Anna Straatman-Iwanowska(University of Birmingham), Andreas Zaucker(University of Birmingham), Yoshiyuki Wakabayashi(National Institutes of Health), Christopher K Bruce(University of Birmingham), Guanmei Luo(University of Birmingham), Fatimah Rahman(University of Birmingham), Figen Gürakan(Hacettepe University), Eda Ütine(Hacettepe University), Tanju Özkan(Bursa Uludağ Üni̇versi̇tesi̇), Jonas Denecke(University of Rostock), Jurica Vuković(University Hospital Centre Zagreb), Maja Di Rocco(Istituto Giannina Gaslini), Hanna Mandel(Meyer Children's Hospital), Hakan Cangül(Bursa Uludağ Üni̇versi̇tesi̇), Randolph P. Matthews(Children's Hospital of Philadelphia), Steven G. Thomas(University of Birmingham), Joshua Z. Rappoport(University of Birmingham), Irwin M. Arias(National Institutes of Health), Hartwig Wolburg(University of Tübingen), A. S. Knisely(King's College Hospital), Déirdre Kelly(Birmingham Children's Hospital), Ferenc Müller(University of Birmingham), Eamonn R. Maher(Birmingham Women's Hospital), Paul Gissen(Birmingham Children's Hospital)
Cited by 180Open Access