Van De Weghe et al., 2017
- Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.
American journal of human genetics
101(1):23-36
Full text @ Am. J. Hum. Genet.
| Human Disease | Fish | Environment | Evidence Code |
|---|---|---|---|
| Joubert syndrome |