Polymorphisms in protamine 1 and 2 genes in asthenozoospermic men: A case-control study

BACKGROUND: Asthenozoospermia is one of the etiologies for male factor infertility. It was shown that any abnormality in protamines genes, reduction of protamines transcript and protamines deficiency may play a key role in asthenozoospermia. OBJECTIVE: The aim of the current study was the evaluation...

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Detalles Bibliográficos
Autores principales: Nabi, Ali, Khalili, Mohammad Ali, Moshrefi, Mojgan, Sheikhha, Mohammad Hasan, Zare Mehrjardi, Ehsan, Ashrafzadeh, Hamid Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research and Clinical Center for Infertility 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6079313/
https://www.ncbi.nlm.nih.gov/pubmed/30123866

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6079313/
https://www.ncbi.nlm.nih.gov/pubmed/30123866

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