IRF2BPL gene mutation: Underlying intellectual disability
收藏NIAID Data Ecosystem2026-03-13 收录
下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA874333
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资源简介：
Our study is first report of the IRF2BPL mutation in intellectual disability patients, including a heterozygous missense mutation: NM_024496.3:c.1313C>A. the Xp22.13-p21.3 duplication and the IRF2BPL mutation may be the genetic etiology of this family with intellectual disability.
创建时间：
2022-08-28
