The prevalence of common CFTR gene mutations and polymorphisms in infertile Iranian men with very severe oligozoospermia

Due to progress in infertility etiology, several genetic bases of infertility are revealed today. This study aimed to investigate the distribution of mutations in the CFTR gene, M470V polymorphism, and IVS8 poly T. Furthermore, we aimed to examine the hotspot exons (4, 7, 9, 10, 11, 20, and 21 exons...

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Detalles Bibliográficos
Autores principales: Jafari, Leyla, Safinejad, Kyumars, Nasiri, Mahboobeh, Heidari, Mansour, Houshmand, Massoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Carol Davila University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126445/
https://www.ncbi.nlm.nih.gov/pubmed/35646184
http://dx.doi.org/10.25122/jml-2021-0261

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9126445/
https://www.ncbi.nlm.nih.gov/pubmed/35646184
http://dx.doi.org/10.25122/jml-2021-0261

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