Screening of Two Neighboring CFTR Mutations in Iranian Infertile Men with Non-Obstructive Azoospermia

The genetic association between cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations and male infertility due to congenital bilateral absence of vas deferens (CBAVD) is well established. Mutant CFTR, however may also be involved in the etiology of male infertility in non-CBAVD c...

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Detalles Bibliográficos
Autores principales: Heidari, Somayeh, Hojati, Zohreh, Motovali-Bashi, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2017
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134755/
https://www.ncbi.nlm.nih.gov/pubmed/28042420

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5134755/
https://www.ncbi.nlm.nih.gov/pubmed/28042420

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