CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis
CEP162 缺陷会导致人类视网膜变性,并揭示其在纤毛发生和神经发生中的双重作用
期刊:Journal of Clinical Investigation
影响因子:13.6
doi:10.1172/JCI161156
Nuzhat, Nafisa; Van Schil, Kristof; Liakopoulos, Sandra; Bauwens, Miriam; Rey, Alfredo Dueñas; Käseberg, Stephan; Jäger, Melanie; Willer, Jason R; Winter, Jennifer; Truong, Hanh M; Gruartmoner, Nuria; Van Heetvelde, Mattias; Wolf, Joachim; Merget, Robert; Grasshoff-Derr, Sabine; Van Dorpe, Jo; Hoorens, Anne; Stöhr, Heidi; Mansard, Luke; Roux, Anne-Françoise; Langmann, Thomas; Dannhausen, Katharina; Rosenkranz, David; Wissing, Karl M; Van Lint, Michel; Rossmann, Heidi; Häuser, Friederike; Nürnberg, Peter; Thiele, Holger; Zechner, Ulrich; Pearring, Jillian N; De Baere, Elfride; Bolz, Hanno J