Whole‐genome sequencing identifies new candidate genes for nonobstructive azoospermia

BACKGROUND: Genetic causes that lead to spermatogenetic failure in patients with nonobstructive azoospermia (NOA) have not been yet completely established. OBJECTIVE: To identify low‐frequency NOA‐associated single nucleotide variants (SNVs) using whole‐genome sequencing (WGS). MATERIALS AND METHODS...

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Detalles Bibliográficos
Autores principales: Malcher, Agnieszka, Stokowy, Tomasz, Berman, Andrea, Olszewska, Marta, Jedrzejczak, Piotr, Sielski, Dawid, Nowakowski, Adam, Rozwadowska, Natalia, Yatsenko, Alexander N., Kurpisz, Maciej K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826517/
https://www.ncbi.nlm.nih.gov/pubmed/36017582
http://dx.doi.org/10.1111/andr.13269

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826517/
https://www.ncbi.nlm.nih.gov/pubmed/36017582
http://dx.doi.org/10.1111/andr.13269

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