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Mechanistic insights into acephalic spermatozoa syndrome–associated mutations in the human SUN5 gene
Acephalic spermatozoa syndrome has been reported for many decades; it is characterized by very few intact spermatozoa and tailless sperm heads in the semen and causes severe male infertility. The only gene in which mutations have been found to be associated with this syndrome encodes Sad1 and UNC84...
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| Vydáno v: | J Biol Chem |
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| Hlavní autoři: | , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Biochemistry and Molecular Biology
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5818197/ https://ncbi.nlm.nih.gov/pubmed/29298896 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.RA117.000861 |
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