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
Hlavní autoři: Shang, Yongliang, Yan, Jie, Tang, Wenhao, Liu, Chao, Xiao, Sai, Guo, Yueshuai, Yuan, Li, Chen, Liang, Jiang, Hui, Guo, Xuejiang, Qiao, Jie, Li, Wei
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society for Biochemistry and Molecular Biology 2018
Témata:
Developmental Biology
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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