Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19
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author: Sophie Saunier, Patrick Nitschké, Christine Bôle-Feysot, Christian Gilissen, Cécile Jeanpierre, Sabine Leh, Joris A Veltman, Alexander Hoischen, Nine V. A. M. Knoers, Rolph Pfundt, Emilie Filhol, Machteld M Oud, Heleen ter Meulen, Irene Stolte-Dijkstra, Cecilie Bredrup, Helge Boman, Eyvind Rødahl, Per M Knappskog, Ben Hamel
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