Cargando…
Cystic fibrosis gene mutations and polymorphisms in Saudi men with infertility
BACKGROUND: Some mutations of the cystic fibrosis transmembrane regulator (CFTR) gene may impair spermatogenesis or cause a congenital absence of the vas deferens that manifests as isolated male infertility. OBJECTIVE: Assess the frequency and analyze the spectrum of CFTR gene variations in Saudi me...
Autores principales: | AlMaghamsi, Talal, Iqbal, Naeem, Al-Esaei, Nabil Abdullrahman, Mohammed, Muhsina, Eddin, Kamel Zein, Ghurab, Fatima, Moghrabi, Nabil, Heaphy, Emily, Junaid, Islam |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
King Faisal Specialist Hospital and Research Centre
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7410224/ https://www.ncbi.nlm.nih.gov/pubmed/32757986 http://dx.doi.org/10.5144/0256-4947.2020.321 |
Ejemplares similares
-
Geographic distribution of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Saudi Arabia
por: Banjar, Hanaa, et al.
Publicado: (2021) -
Genotype patterns for mutations of the cystic fibrosis transmembrane conductance regulator gene: a retrospective descriptive study from Saudi Arabia
por: Banjar, Hanaa Hasan, et al.
Publicado: (2020) -
The first case report of double homozygous of 2 different mutations in the CFTR gene in Saudi Arabia
por: Banjar, Hanaa, et al.
Publicado: (2017) -
Acute respiratory failure and generalized hypotonia secondary to vitamin D dependent rickets type 1A
por: Ahmad, Noman, et al.
Publicado: (2018) -
EFFICIENCY VERSUS EFFECTIVENESS OF THE SAUDI FAMILY DOCTOR
por: Al Kurashi, Nabil Y.
Publicado: (2004)