KHDC3L mutation causes recurrent pregnancy loss by inducing genomic instability of human early embryonic cells

Recurrent pregnancy loss (RPL) is an important complication in reproductive health. About 50% of RPL cases are unexplained, and understanding the genetic basis is essential for its diagnosis and prognosis. Herein, we report causal KH domain containing 3 like (KHDC3L) mutations in RPL. KHDC3L is expr...

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Detalles Bibliográficos
Autores principales: Zhang, Weidao, Chen, Zhongliang, Zhang, Dengfeng, Zhao, Bo, Liu, Lu, Xie, Zhengyuan, Yao, Yonggang, Zheng, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812846/
https://www.ncbi.nlm.nih.gov/pubmed/31609975
http://dx.doi.org/10.1371/journal.pbio.3000468

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812846/
https://www.ncbi.nlm.nih.gov/pubmed/31609975
http://dx.doi.org/10.1371/journal.pbio.3000468

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