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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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| 出版年: | PLoS One |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Public Library of Science
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5634651/ https://ncbi.nlm.nih.gov/pubmed/29016666 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0186149 |
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