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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...
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| Publicado no: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7336754/ https://ncbi.nlm.nih.gov/pubmed/32410354 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1284 |
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