Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to Study the Etiology of Non-Obstructive Azoospermia: Demonstration of the Dispensable Role of the Testis-Specific Genes C1orf185 and CCT6B

The genetic landscape of male infertility is highly complex. It is estimated that at least 4000 genes are involved in human spermatogenesis, but only few have so far been extensively studied. In this study, we investigated by whole exome sequencing two cases of idiopathic non-obstructive azoospermia...

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Detalles Bibliográficos
Autores principales: Cazin, Caroline, Neirijnck, Yasmine, Loeuillet, Corinne, Wehrli, Lydia, Kühne, Françoise, Lordey, Isabelle, Mustapha, Selima Fourati Ben, Bouker, Amin, Zouari, Raoudha, Thierry-Mieg, Nicolas, Nef, Serge, Arnoult, Christophe, Ray, Pierre F., Kherraf, Zine-Eddine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750304/
https://www.ncbi.nlm.nih.gov/pubmed/35011680
http://dx.doi.org/10.3390/cells11010118

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750304/
https://www.ncbi.nlm.nih.gov/pubmed/35011680
http://dx.doi.org/10.3390/cells11010118

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