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CHD7 missense variants and clinical characteristics of Chinese males with infertility
BACKGROUND: Isolated hypogonadotropic hypogonadism (IHH) and Kallmann syndrome (KS) are rare genetic diseases that cause male infertility. The chromodomain helicase DNA‐binding protein 7 (CHD7) gene is commonly associated with KS and IHH. We speculated that CHD7 variants may be associated with male...
Autores principales: | Li, Leilei, Wang, Ruixue, Yu, Yang, Zhang, Hongguo, Jiang, Yuting, Yang, Xiao, Liu, Ruizhi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503206/ https://www.ncbi.nlm.nih.gov/pubmed/32573075 http://dx.doi.org/10.1002/mgg3.1372 |
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