Cargando…
Exon 10 CFTR gene mutation in male infertility
Background: About 10% of infertilities with obstructive azoospermia are congenital and caused by CF gene mutations. M469I mutation was observed for the first time in Taiwanese patients. This mutation not only causes CF, but also may be the origin of infertility too. Objective: In this study, we aime...
Autores principales: | Hojati, Zohreh, Heidari, Somaye, Motovali-Bashi, Majid |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research and Clinical Center for Infertility
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165948/ https://www.ncbi.nlm.nih.gov/pubmed/25246892 |
Ejemplares similares
-
Screening of Two Neighboring CFTR Mutations in Iranian
Infertile Men with Non-Obstructive Azoospermia
por: Heidari, Somayeh, et al.
Publicado: (2017) -
Association between polymorphisms of exon 12 and exon 24 of JHDM2A gene and male infertility
por: Hojati, Zohreh, et al.
Publicado: (2016) -
The stromelysin-1 5A/5A genotype enhances colorectal cancer cell invasion in Iranian population
por: Motovali-Bashi, Majid, et al.
Publicado: (2012) -
Molecular Analysis of the Clavulanic Acid Regulatory
Gene Isolated from an Iranian Strain of Streptomyces
Clavuligerus , PTCC 1709
por: Hojati, Zohreh, et al.
Publicado: (2011) -
Association between Serum Paraoxonase 1 Activities (PONase/AREase) and L55M Polymorphism in Risk of Female Infertility
por: Motovali-Bashi, Majid, et al.
Publicado: (2015)