Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans
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author: Nicholas Katsanis, Friedhelm Hildebrandt, Sophie Saunier, Christine Bôle-Feysot, Hülya Kayserili, Patrick Nitschké, Albane A Bizet, Daniela A Braun, Anna Lehman, Miriam Schmidts, Emma L. Duncan, Edgar A. Otto, Matthew A. Brown, Peter J Scambler, Steven Jones, Stephane Burtey, Peter Trnka, Heon Yung Gee, Eamonn R Maher, Toby Hurd, Jan Halbritter, Rannar Airik, Markus Schueler, Jonathan D Porath, Pauline Krug, Emilie Filhol, Peter G. Czarnecki, Michel R Leroux, Khemchand Netaram Moorani, Beyhan Tuysuz, Bertrand Knebelmann, Aideen M McInerney-Leo, Daniel Doherty
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