Cargando…
Association of CATSPER1, SPATA16 and TEX11 genes polymorphism with idiopathic azoospermia and oligospermia risk in Iranian population
BACKGROUND: Male infertility is a heterogeneous disease which can occur due to spermatogenesis defects. The idiopathic azoospermia and oligospermia are the common cause of male infertility with unknown underlying molecular mechanisms. The aim of this study was to investigate association of idiopathi...
Autores principales: | Behvarz, Mohammadreza, Rahmani, Seyyed Ali, Siasi Torbati, Elham, Danaei Mehrabad, Shahla, Bikhof Torbati, Maryam |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897944/ https://www.ncbi.nlm.nih.gov/pubmed/35248021 http://dx.doi.org/10.1186/s12920-022-01197-w |
Ejemplares similares
-
The Prevalence of Y Chromosome Microdeletions
in Iranian Infertile Men with Azoospermia
and Severe Oligospermia
por: Asadi, Fahimeh, et al.
Publicado: (2017) -
Y chromosome microdeletions frequency in idiopathic azoospermia, oligoasthenozoospermia, and oligospermia
por: Gholami, Delnya, et al.
Publicado: (2017) -
Distal Renal Tubular Acidosis in an Iranian Patient with Hereditary Spherocytosis
por: Shahab-Movahed, Zahra, et al.
Publicado: (2021) -
Association study of six SNPs in PRM1, PRM2 and TNP2 genes in iranian infertile men with idiopathic azoospermia
por: Siasi, Elham, et al.
Publicado: (2012) -
Copy number variations (CNVs) and karyotyping analysis in males with azoospermia and oligospermia
por: Xin, Xing, et al.
Publicado: (2023)