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Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans
Human infertility is a multifactorial disease that affects 8%–12% of reproductive-aged couples worldwide. However, the genetic causes of human infertility are still poorly understood. Synaptonemal complex (SC) is a conserved tripartite structure that holds homologous chromosomes together and plays a...
Autores principales: | Fan, Suixing, Jiao, Yuying, Khan, Ranjha, Jiang, Xiaohua, Javed, Abdul Rafay, Ali, Asim, Zhang, Huan, Zhou, Jianteng, Naeem, Muhammad, Murtaza, Ghulam, Li, Yang, Yang, Gang, Zaman, Qumar, Zubair, Muhammad, Guan, Haiyang, Zhang, Xingxia, Ma, Hui, Jiang, Hanwei, Ali, Haider, Dil, Sobia, Shah, Wasim, Ahmad, Niaz, Zhang, Yuanwei, Shi, Qinghua |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895996/ https://www.ncbi.nlm.nih.gov/pubmed/33508233 http://dx.doi.org/10.1016/j.ajhg.2021.01.010 |
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