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.
CRISPR List (2 Records)
Target Reagent
ccdc32 CRISPR1-ccdc32
CRISPR2-ccdc32