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Journal: Genes, 2022
Volume: 13
Number: 1558

Article: Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome due to a Novel Nonsense Mutation in the ZC4H2 Gene
Authors: by Jing-Jing Sun, Qin Cai, Miao Xu, Yan-Na Liu, Wan-Rui Li, Juan Li, Li Ma, Cheng Cai, Xiao-Hui Gong, Yi-Tao Zeng, Zhao-Rui Ren and Fanyi Zeng
Link: https://www.mdpi.com/2073-4425/13/9/1558

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