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Amendments and Corrections |
Correction: Corrigendum: 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 Özkan
- , Jonas Denecke
- , Jurica Vukovic
- , Maja Di Rocco
- , Hanna Mandel
- , Hakan Cangul
- , Randolph P Matthews
- , Steve G Thomas
- , Joshua Z Rappoport
- , Irwin M Arias
- , Hartwig Wolburg
- , A S Knisely
- , Deirdre A Kelly
- , Ferenc Müller
- , Eamonn R Maher
- & Paul Gissen
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Research |
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
- Ursula M Smith
- , Mark Consugar
- , Louise J Tee
- , Brandy M McKee
- , Esther N Maina
- , Shelly Whelan
- , Neil V Morgan
- , Erin Goranson
- , Paul Gissen
- , Stacie Lilliquist
- , Irene A Aligianis
- , Christopher J Ward
- , Shanaz Pasha
- , Rachaneekorn Punyashthiti
- , Saghira Malik Sharif
- , Philip A Batman
- , Christopher P Bennett
- , C Geoffrey Woods
- , Carole McKeown
- , Martine Bucourt
- , Caroline A Miller
- , Phillip Cox
- , Lihadh AlGazali
- , Richard C Trembath
- , Vicente E Torres
- , Tania Attie-Bitach
- , Deirdre A Kelly
- , Eamonn R Maher
- , Vincent H Gattone II
- , Peter C Harris
- & Colin A Johnson
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Research |
Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis–renal dysfunction–cholestasis (ARC) syndrome
- Paul Gissen
- , Colin A Johnson
- , Neil V Morgan
- , Janneke M Stapelbroek
- , Tim Forshew
- , Wendy N Cooper
- , Patrick J McKiernan
- , Leo W J Klomp
- , Andrew A M Morris
- , James E Wraith
- , Patricia McClean
- , Sally A Lynch
- , Richard J Thompson
- , Bryan Lo
- , Oliver W Quarrell
- , Maja Di Rocco
- , Richard C Trembath
- , Hanna Mandel
- , S Wali
- , Fiona E Karet
- , A S Knisely
- , Roderick H J Houwen
- , Deirdre A Kelly
- & Eamonn R Maher
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Research |
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 Özkan
- , Jonas Denecke
- , Jurica Vukovic
- , Maja Di Rocco
- , Hanna Mandel
- , Hakan Cangul
- , Randolph P Matthews
- , Steve G Thomas
- , Joshua Z Rappoport
- , Irwin M Arias
- , Hartwig Wolburg
- , A S Knisely
- , Deirdre A Kelly
- , Ferenc Müller
- , Eamonn R Maher
- & Paul Gissen
