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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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| Publicado en: | J Assist Reprod Genet |
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| Autores principales: | , , , , , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Springer US
2021
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| Materias: | |
| Acceso en línea: | 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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