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Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice
Male infertility is a major concern affecting human reproductive health. Asthenoteratospermia can cause male infertility through reduced motility and abnormal morphology of spermatozoa. Several genes, including DNAH1 and some CFAP family members, are involved in multiple morphological abnormalities...
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| Vydáno v: | Am J Hum Genet |
|---|---|
| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Elsevier
2019
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6451729/ https://ncbi.nlm.nih.gov/pubmed/30929735 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2019.02.020 |
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