Homo sapiens Exome
收藏NIAID Data Ecosystem2026-05-02 收录
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https://www.ncbi.nlm.nih.gov/sra/SRP564205
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资源简介：
The whole exome sequencing results suggested compound heterozygous mutations of DIAPH1 (c.1051C>T, p.R351X,922; c.609delA, p.E203E fs*19), and were correlated with the complex syndrome.
创建时间：
2025-02-19
