Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome due to a Novel Nonsense Mutation in the ZC4H2 Gene

por Sun, Jing-Jing, Cai, Qin, Xu, Miao, Liu, Yan-Na, Li, Wan-Rui, Li, Juan, Ma, Li, Cai, Cheng, Gong, Xiao-Hui, Zeng, Yi-Tao, Ren, Zhao-Rui, Zeng, Fanyi
Publicado 2022