Xu, M;    Xie, YA;    Abouzeid, H;    Gordon, CT;    Fiorentino, A;    Sun, Z;    Lehman, A;                                                                                                                                                                                     ... Schorderet, DF; + view all <#>        Xu, M;  Xie, YA;  Abouzeid, H;  Gordon, CT;  Fiorentino, A;  Sun, Z;  Lehman, A;  Osman, IS;  Dharmat, R;  Riveiro-Alvarez, R;  Bapst-Wicht, L;  Babino, D;  Arno, G;  Busetto, V;  Zhao, L;  Li, H;  Lopez-Martinez, MA;  Azevedo, LF;  Hubert, L;  Pontikos, N;  Eblimit, A;  Lorda-Sanchez, I;  Kheir, V;  Plagnol, V;  Oufadem, M;  Soens, ZT;  Yang, L;  Bole-Feysot, C;  Pfundt, R;  Allaman-Pillet, N;  Nitschké, P;  Cheetham, ME;  Lyonnet, S;  Agrawal, SA;  Li, H;  Pinton, G;  Michaelides, M;  Besmond, C;  Li, Y;  Yuan, Z;  von Lintig, J;  Webster, AR;  Le Hir, H;  Stoilov, P;  UK Inherited Retinal Dystrophy Consortium, .;  Amiel, J;  Hardcastle, AJ;  Ayuso, C;  Sui, R;  Chen, R;  Allikmets, R;  Schorderet, DF;   - view fewer <#>    (2017)    Mutations in the Spliceosome Component CWC27 Cause Retinal Degeneration with or without Additional Developmental Anomalies.                   American Journal of Human Genetics , 100  (4)   pp. 592-604.    10.1016/j.ajhg.2017.02.008 <https://doi.org/10.1016/j.ajhg.2017.02.008>.       Green open access