Beck et al., 2014
- Mutation of POC1B in a Severe Syndromic Retinal Ciliopathy.
Human Mutation
35(10):1153-62
Full text @ Hum. Mutat.
| Human Disease | Fish | Environment | Evidence Code |
|---|---|---|---|
| autosomal dominant polycystic kidney disease | |||
| ciliopathy | |||
| Joubert syndrome |