| 1 | RP35, SEMA4A |
| A point mutation in Semaphorin 4A associates with defective endosomal sorting and causes retinal degeneration. | |
| Nojima S, Toyofuku T, Kamao H, Ishigami C, Kaneko J, Okuno T, Takamatsu H, Ito D, Kang S, Kimura T, Yoshida Y, Morimoto K, Maeda Y, Ogata A, Ikawa M, Morii E, Aozasa K, Takagi J, Takahashi M, Kumanogoh A. | |
| Nat Commun 4:1406. doi: 10.1038/ncomms2420. 2013 | |
| 2 | CORD10,RP35,SEMA4A |
| Identification of novel mutations in SEMA4A gene associated with retinal degenerative diseases. | |
| Abid A, Ismail M, Mehdi SQ, Khaliq S. | |
| J Med Genet [Epub ahead of print] 2005 | |