A homozygous loss-of-function mutation in FBXO43 causes human non-obstructive azoospermia.
Wu H, Zhang X, Shen Q, Liu Y, Gao Y, Wang G, Lv M, Hua R, Xu Y, Zhou P, Wei Z, Tao F, He X, Cao Y, Liu M.
Wu H, et al. Among authors: cao y.
Clin Genet. 2022 Jan;101(1):55-64. doi: 10.1111/cge.14069. Epub 2021 Oct 11.
Clin Genet. 2022.
PMID: 34595750