A novel loss-of-function SYCP2 variant causes asthenoteratozoospermia in infertile males

Background:Infertility is a multiplex disorder in the reproductive system. Unexplained infertility affects 2%-3% of reproductive-aged couples. Male factors contribute to about half of all infertility cases. About 15% of these cases are predicted to have a genetic etiology. With the wide application...

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Principais autores:	Cong Liu, Yinfeng Zhang, Youming Zhao, Haining Luo
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Frontiers Media S.A. 2025-05-01
coleção:	Frontiers in Genetics
Assuntos:	male infertility whole exome sequence SYCP2 gene variation mini-gene splicing assay
Acesso em linha:	https://www.frontiersin.org/articles/10.3389/fgene.2025.1595720/full
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