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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...
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| Publié dans: | Mol Genet Genomic Med |
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| Auteurs principaux: | , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
John Wiley and Sons Inc.
2020
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7503206/ https://ncbi.nlm.nih.gov/pubmed/32573075 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1372 |
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