Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders

STUDY QUESTION: What are the causative genetic variants in patients with male infertility due to severe sperm motility disorders? SUMMARY ANSWER: We identified high confidence disease-causing variants in multiple genes previously associated with severe sperm motility disorders in 10 out of 21 patien...

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Detalles Bibliográficos
Autores principales: Oud, M S, Houston, B J, Volozonoka, L, Mastrorosa, F K, Holt, G S, Alobaidi, B K S, deVries, P F, Astuti, G, Ramos, L, Mclachlan, R I, O’Bryan, M K, Veltman, J A, Chemes, H E, Sheth, H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373475/
https://www.ncbi.nlm.nih.gov/pubmed/34089056
http://dx.doi.org/10.1093/humrep/deab099

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8373475/
https://www.ncbi.nlm.nih.gov/pubmed/34089056
http://dx.doi.org/10.1093/humrep/deab099

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