Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome due to a Novel Nonsense Mutation in the ZC4H2 Gene. - Sun JJ; Cai Q; Xu M; Liu YN; Li WR; Li J; Ma L; Cai C; Gong XH; Zeng YT; Ren ZR; Zeng F (Genes, 2022)