Van De Weghe, J. C., Rusterholz, T. D., Latour, B., Grout, M. E., Aldinger, K. A., Shaheen, R., . . . Doherty, D. (2017). Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish. Am J Hum Genet.

Van De Weghe, Julie C., et al. "Mutations in ARMC9, Which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish." Am J Hum Genet 2017.

Van De Weghe, Julie C., et al. "Mutations in ARMC9, Which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish." Am J Hum Genet 2017.