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

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.W genetic variants were reported to be involved i...

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Detalles Bibliográficos
Autores principales: Haji Ebrahim Zargar, Haleh, Mohseni Meybodi, Anahita, Sabbaghian, Marjan, Shahhoseini, Maryam, Asadpor, Ummulbanin, Sadighi Gilani, Mohammad Ali, Chehrazi, Mohammad, Farhangniya, Mansoureh, Shahzadeh Fazeli, Seyed Abolhassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518489/
https://www.ncbi.nlm.nih.gov/pubmed/26246879

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518489/
https://www.ncbi.nlm.nih.gov/pubmed/26246879

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