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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...
Autores principales: | Kherraf, Zine-Eddine, Cazin, Caroline, Lestrade, Florence, Muronova, Jana, Coutton, Charles, Arnoult, Christophe, Thierry-Mieg, Nicolas, Ray, Pierre F |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
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 |
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