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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Publicat a:Sci Rep
Autors principals: D’Aurora, Marco, Ferlin, Alberto, Garolla, Andrea, Franchi, Sara, D’Onofrio, Laura, Trubiani, Oriana, Palka, Giandomenico, Foresta, Carlo, Stuppia, Liborio, Gatta, Valentina
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group 2017
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Article
Accés en línia: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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