Whole exome sequencing identified a homozygous novel variant in DOP1A gene in the Pakistan family with neurodevelopmental disabilities
收藏NIAID Data Ecosystem2026-05-01 收录
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资源简介：
Our study reveals the potential pathway of the myelinogenesis relevant NDDs and identifies DOP1A as a potential NDDs-relevant gene in human.
创建时间：
2023-10-11
