Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only Syndrome

A genetic origin is estimated in 30% of infertile men with the common phenotypes of oligo- or azoospermia, but the pathogenesis of spermatogenic failure remains frequently obscure. To determine the involvement of Copy Number Variants (CNVs) in the origin of male infertility, patients with idiopathic...

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Detalles Bibliográficos
Autores principales: Tüttelmann, Frank, Simoni, Manuela, Kliesch, Sabine, Ledig, Susanne, Dworniczak, Bernd, Wieacker, Peter, Röpke, Albrecht
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084853/
https://www.ncbi.nlm.nih.gov/pubmed/21559371
http://dx.doi.org/10.1371/journal.pone.0019426

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084853/
https://www.ncbi.nlm.nih.gov/pubmed/21559371
http://dx.doi.org/10.1371/journal.pone.0019426

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