Functional Analysis of MEIS2
收藏NIAID Data Ecosystem2026-05-10 收录
下载链接：
https://www.ncbi.nlm.nih.gov/sra/SRP619059
下载链接
链接失效反馈官方服务：
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
