CEP162 deficiency causes human retinal degeneration and reveals a dual role inciliogenesis and neurogenesis
Nafisa Nuzhat, Kristof Van Schil, Sandra Liakopoulos, Miriam Bauwens, Alfredo Dueñas Rey, Stephan Käseberg, Melanie Jäger, Jason R. Willer, Jennifer Winter, Hanh M. Truong, Núria Gruartmoner Roura, Mattias Van Heetvelde, Joachim Wolf, Robert Merget, Sabine Grasshoff‐Derr, , Hanno J. Bolz
The paper shows that CEP162 deficiency causes retinal degeneration by impairing ciliary function, while retaining a role in neurogenesis.
Journal of Clinical Investigation · Mar 2, 2023Peer-reviewedGenetics