Association of Two Polymorphisms in H2B.W Gene with Azoospermia and Severe Oligozoospermia in An Iranian Population

Autor: Haji Ebrahim Zargar, H., Mohseni Meybodi, A., Sabbaghian, M., Shahhoseini, M., Asadpor, U., Sadighi Gilani, M. A., Chehrazi, M., Farhangniya, M., seyed abolhassan shahzadeh fazeli

Publikováno v: International Journal of Fertility & Sterility
Scopus-Elsevier
International Journal of Fertility and Sterility, Vol 9, Iss 2, Pp 205-214 (2015)

Background During spermatogenesis, the H2B family, member W (H2B.W) gene, en- codes a testis specific histone that is co-localized with telomeric sequences and has the potential role to mediate the sperm-specific chromatin remodeling. Previously H2B.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::cb6b7f0752c9a29ac5810e845fc92ab2
https://pubmed.ncbi.nlm.nih.gov/26246879