SCN1A truncation-positive Dravet syndrome exomes
收藏NIAID Data Ecosystem2026-03-10 收录
下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA391353
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资源简介：
To identify modifier gene variants that contribute to clinical outcome, we sequenced the exomes of individuals at both ends of a phenotype distribution (i.e., mild and severe cognitive condition).
创建时间：
2017-06-21
