Fam47c-KO 基因敲除小鼠

1. Malcher, Agnieszka, Stokowy, Tomasz, Berman, Andrea, Yatsenko, Alexander N, Kurpisz, Maciej K. 2022. Whole-genome sequencing identifies new candidate genes for nonobstructive azoospermia. In Andrology, 10, 1605-1624. doi:10.1111/andr.13269. https://pubmed.ncbi.nlm.nih.gov/36017582/

2. Chertman, Willy, Arora, Himanshu, Griswold, Anthony J, Lopategui, Diana M, Ramasamy, Ranjith. 2019. Whole Exome Sequencing Identifies a Rare Nonsense Mutation in FAM47C as a Possible Cause of Severe Oligospermia in Brothers With Varicocele. In Urology, 129, 71-73. doi:10.1016/j.urology.2019.03.016. https://pubmed.ncbi.nlm.nih.gov/30922974/