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A putative human infertility allele of the meiotic recombinase DMC1 does not affect fertility in mice

Whole-exome or whole-genome sequencing is becoming routine in clinical situations for identifying mutations underlying presumed genetic causes of disease including infertility. While this is a powerful approach for implicating polymorphisms or de novo mutations in genes plausibly related to the phen...

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Bibliografske podrobnosti
izdano v:Hum Mol Genet
Main Authors: Tran, Tina N, Schimenti, John C
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2018
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6216207/
https://ncbi.nlm.nih.gov/pubmed/30085085
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy286
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