A systematic review of the validated monogenic causes of human male infertility: 2020 update and a discussion of emerging gene–disease relationships

BACKGROUND: Human male infertility has a notable genetic component, including well-established diagnoses such as Klinefelter syndrome, Y-chromosome microdeletions and monogenic causes. Approximately 4% of all infertile men are now diagnosed with a genetic cause, but a majority (60–70%) remain withou...

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Detalles Bibliográficos
Autores principales: Houston, Brendan J, Riera-Escamilla, Antoni, Wyrwoll, Margot J, Salas-Huetos, Albert, Xavier, Miguel J, Nagirnaja, Liina, Friedrich, Corinna, Conrad, Don F, Aston, Kenneth I, Krausz, Csilla, Tüttelmann, Frank, O’Bryan, Moira K, Veltman, Joris A, Oud, Manon S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8730311/
https://www.ncbi.nlm.nih.gov/pubmed/34498060
http://dx.doi.org/10.1093/humupd/dmab030

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8730311/
https://www.ncbi.nlm.nih.gov/pubmed/34498060
http://dx.doi.org/10.1093/humupd/dmab030

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