Whole-exome sequencing
收藏NIAID Data Ecosystem2026-03-14 收录
下载链接：
https://doi.org/10.7910/DVN/3A55HE
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资源简介：
Sequencing of coding regions of genes associated with known clinical conditions. For the purpose of the analysis, only genes related to the clinical indication ADAR, CA2 COL4A1,CTC1, ERCC6, ERCC8, GALC, IFIH1, MYORG, PDGFB, PDGFRB, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, SLC20A2, TREM2, TREX1, TYROBP, XPR1, ISG15, PSMB8, SLC46A1, USP18 were examined
创建时间：
2023-03-12
