From azoospermia to macrozoospermia, a phenotypic continuum due to mutations in the ZMYND15 gene

Thanks to tremendous advances in sequencing technologies and in particular to whole exome sequencing (WES), many genes have now been linked to severe sperm defects. A precise genetic diagnosis is obtained for a minority of patients and only for the most severe defects like azoospermia or macrozoospe...

Descripción completa

Detalles Bibliográficos
Autores principales: Kherraf, Zine-Eddine, Cazin, Caroline, Lestrade, Florence, Muronova, Jana, Coutton, Charles, Arnoult, Christophe, Thierry-Mieg, Nicolas, Ray, Pierre F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Invited Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9226687/
https://www.ncbi.nlm.nih.gov/pubmed/35017390
http://dx.doi.org/10.4103/aja202194

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9226687/
https://www.ncbi.nlm.nih.gov/pubmed/35017390
http://dx.doi.org/10.4103/aja202194

Ejemplares similares