A novel autism-associated UBLCP1 mutation impacts proteasome regulation/activity
收藏NIAID Data Ecosystem2026-05-01 收录
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资源简介：
A novel UBLCP1 mutation is identified in a Lebanese family with ASD resulting in a premature stop codon that disrupts UBLCP1 protein phosphatase domain disturbing proteasome regulation and activity.
创建时间：
2023-11-30
