Harel et al., 2020
- Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies.
Human molecular genetics
29(9):1489-1497
Full text @ Hum. Mol. Genet.
Target | Reagent |
---|---|
ccdc32 | CRISPR1-ccdc32 |
CRISPR2-ccdc32 |