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Loss‐of‐function mutation in TSGA10 causes acephalic spermatozoa phenotype in human
BACKGROUND: Acephalic spermatozoa is an extremely rare type of teratozoospermia that is associated with male infertility. Several genes have been reported to be relevant to acephalic spermatozoa. Thus, more genetic pathogenesis needs to be explored. METHODS: Whole‐exome sequencing was performed in a...
| Autores principales: | , , , , , , , , , , |
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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/PMC7336754/ https://www.ncbi.nlm.nih.gov/pubmed/32410354 http://dx.doi.org/10.1002/mgg3.1284 |