Citations for
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