| 1 | CCNOA, TDRD7 |
| Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans. | |
| Tan YQ, Tu C, Meng L, Yuan S, Sjaarda C, Luo A, Du J, Li W, Gong F, Zhong C, Deng HX, Lu G, Liang P, Lin G. | |
| Genet Med enet Med. 2017 Aug 24. doi: 10.1038/gim.2017.130. [Epub ahead of print] 2017 | |