GeneticsJournal of Clinical InvestigationPeer-reviewed
CEP162 deficiency causes human retinal degeneration and reveals a dual role inciliogenesis and neurogenesis
Nafisa Nuzhat, Kristof Van Schil, Sandra Liakopoulos…·Hanno J. Bolz
The paper shows that CEP162 deficiency causes retinal degeneration by impairing ciliary function, while retaining a role in neurogenesis.