Novel Variants in RSA. Homo sapiens
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA325830
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The present study thus involved whole-exome sequencing in unrelated women affected by RSA. Bioinformatics analysis was mainly based on studying non-synonymous sequence variants in a subset of RSA candidate genes. These genes belonged to distinct molecular cascades playing key roles in implantation/pregnancy biology and represent potential future biomarkers for RSA.
创建时间:
2016-06-15



