Testis Transcriptome Modulation in Klinefelter Patients with Hypospermatogenesis

The main genetic cause of male infertility is represented by the Klinefelter Syndrome (KS), a condition accounting for 3% of all cases of infertility and up to15% of cases of azoospermia. KS is generally characterized by azoospermia; approximately 10% of cases have severe oligozoospermia. Among thes...

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Vydáno v:Sci Rep
Hlavní autoři: D’Aurora, Marco, Ferlin, Alberto, Garolla, Andrea, Franchi, Sara, D’Onofrio, Laura, Trubiani, Oriana, Palka, Giandomenico, Foresta, Carlo, Stuppia, Liborio, Gatta, Valentina
Médium: Artigo
Jazyk:Inglês
Vydáno: Nature Publishing Group 2017
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5374630/
https://ncbi.nlm.nih.gov/pubmed/28361989
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep45729
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