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New point mutation in Golga3 causes multiple defects in spermatogenesis
repro27 mice exhibit fully penetrant male-specific infertility associated with a nonsense mutation in the golgin subfamily A member 3 gene (Golga3). GOLGA3 is a Golgi complex-associated protein implicated in protein trafficking, apoptosis, positioning of the Golgi, and spermatogenesis. In repro27 mu...
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Main Authors: | , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2013
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4134951/ https://ncbi.nlm.nih.gov/pubmed/23495255 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.2047-2927.2013.00070.x |
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