Whole exome sequencing of Coffin-Siris syndrome patient
收藏NIAID Data Ecosystem2026-03-14 收录
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA902508
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资源简介:
In this study, two additional individuals were diagnosed with CSS caused by BAF mutations by whole exon sequencing.
创建时间:
2022-11-17



