Copy number variants in patients with severe oligozoospermia and Sertoli-cell-only syndrome.

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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Bibliographic Details
Main Authors: Frank Tüttelmann, Manuela Simoni, Sabine Kliesch, Susanne Ledig, Bernd Dworniczak, Peter Wieacker, Albrecht Röpke
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3084853?pdf=render

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