Association of G/T(rs222859) polymorphism in Exon 1 of YBX2 gene with azoospermia, among Iranian infertile males
Author:
Affiliation:
1. Cellular and Molecular Research Center of Qazvin University of Medical Science; Qazvin Iran
2. Fertility and Infertility Center of Shariati Hospital; Tehran Iran
Publisher
Wiley
Subject
Urology,Endocrinology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/and.12537/fullpdf
Reference23 articles.
1. Identification and evaluation of a novel sperm protamine abnormality in a population of infertile males;Aoki;Hum Reprod,2005
2. Altered protamine expression and diminished spermatogenesis: what is the link?;Carrell;Hum Reprod Update,2007
3. Higher frequency of Yq microdeletions in sperm DNA as compared to DNA isolated from blood;Dada;Asian J Androl.,2007
4. Some single nucleotide polymorphisms of MSY2 gene might contribute to susceptibility to spermatogenic impairment in idiopathic infertile men;Deng;Urology,2008
5. Ychromosomal microdeletions and partial deletions of theAzoospermia Factor c (AZFc) region in normozoospermic, severeoligozoospermic and azoospermic men in Sri Lanka;Fernando;Asian J Androl,2006
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