Functional Analysis of MEIS2
收藏NIAID Data Ecosystem2026-05-10 收录
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资源简介：
To identify disease-causing mutations, we performed whole-exome sequencing (WES) of affected family members and subsequently employed a minigene splicing assay to evaluate the functional impact of the MEIS2 gene splicing variant.
创建时间：
2025-09-15
