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A novel splicing variant in DNAH8 causes asthenozoospermia
PURPOSE: To identify the genetic factors responsible for asthenozoospermia, which is a major cause of male infertility characterized by immotile and malformed spermatozoa. METHODS: Whole-exome sequencing was performed in two brothers from a family with asthenozoospermia to identify pathogenic varian...
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| 出版年: | J Assist Reprod Genet |
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| 主要な著者: | , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer US
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8266938/ https://ncbi.nlm.nih.gov/pubmed/33611675 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-021-02116-1 |
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