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Publication : Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.

First Author  Van De Weghe JC Year  2017
Journal  Am J Hum Genet Volume  101
Issue  1 Pages  23-36
PubMed ID  28625504 Mgi Id 
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