https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Mutations in ARMC9, which encodes a basal body protein, cause Joubert syndrome in humans and ciliopathy phenotypes in Zebrafish https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:34260 Thu 03 Feb 2022 12:20:40 AEDT ]]> Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:26556 Sat 24 Mar 2018 07:26:14 AEDT ]]>