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.
Target | Reagent |
---|---|
armc9 | CRISPR1-armc9 |
CRISPR2-armc9 | |
CRISPR3-armc9 | |
CRISPR4-armc9 |