Multi-omics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and non-canonical Wnt signaling dysregulation. Multi-omics of Bohring-Opitz syndrome truncating ASXL1 mutations identify canonical and non-canonical Wnt signaling dysregulation
收藏NIAID Data Ecosystem2026-05-01 收录
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This SuperSeries is composed of the SubSeries listed below. Overall design: Refer to individual Series
创建时间：
2023-04-26
