A novel nonsense mutation in PPP2R5D is associated with neurodevelopmental disorders and shows incomplete penetrance in a Chinese pedigree
A novel nonsense mutation in PPP2R5D is associated with neurodevelopmental disorders and shows incomplete penetrance in a Chinese pedigree
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DOI：
10.1016/j.clineuro.2022.107524
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发表时间：
2022
期刊：
影响因子：
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通讯作者：
Lei Zhang
中科院分区：
文献类型：
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作者：
Ruihong Liu;Yihuan Huang;Chunyi Li;Ping Wang;Yiming Wang;Lei Zhang
