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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...
Gorde:
| Argitaratua izan da: | Mol Genet Genomic Med |
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| Egile Nagusiak: | , , , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
John Wiley and Sons Inc.
2020
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| Gaiak: | |
| Sarrera elektronikoa: | 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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