Novel genes and mutations in patients affected by recurrent pregnancy loss

Recurrent pregnancy loss is a frequently occurring human infertility-related disease affecting ~1% of women. It has been estimated that the cause remains unexplained in >50% cases which strongly suggests that genetic factors may contribute towards the phenotype. Concerning its molecular aetiology...

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Detalles Bibliográficos
Autores principales: Quintero-Ronderos, Paula, Mercier, Eric, Fukuda, Michiko, González, Ronald, Suárez, Carlos Fernando, Patarroyo, Manuel Alfonso, Vaiman, Daniel, Gris, Jean-Christophe, Laissue, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634651/
https://www.ncbi.nlm.nih.gov/pubmed/29016666
http://dx.doi.org/10.1371/journal.pone.0186149

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634651/
https://www.ncbi.nlm.nih.gov/pubmed/29016666
http://dx.doi.org/10.1371/journal.pone.0186149

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