Biblio

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Journal Article

He J, Liu Q, Wang W, Su L, Meng L, Tan C, Zhang H, Zhang Q, Lu G, Du J, et al. Novel homozygous variant of CCIN causes male infertility owing to the abnormal sperm head with a nuclear subsidence phenotype. Clin Genet. 2022.

He J, Su L, Wang W, Li Y, Meng L, Tan C, Lin G, Tan Y-Q, Zhang Q, Chaofeng T. C9orf131 and C10orf120 are not essential for male fertility in humans or mice. Dev Biol. 2023.

Tan C, Meng L, Lv M, He X, Sha Y, Tang D, Tan Y, Hu T, He W, Tu C, et al. Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. Am J Hum Genet. 2021.

Tu C, Cong J, Zhang Q, He X, Zheng R, Yang X, Gao Y, Wu H, Lv M, Gu Y, et al. Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice. Am J Hum Genet. 2021.