Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.
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| Description | scientific article published on 14 June 2017 |
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author: Ruxandra Bachmann-Gagescu William B. Dobyns Kimberly A Aldinger Megan E Grout Daniel Doherty Ranad Shaheen Deborah A Nickerson University of Washington Center for Mendelian Genomics Ohad Birk |
| Publication date | June 15, 2017 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |