Disease-associated mutations impact DNMT1 function through dynamic allosteric effects and solvent exposure
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资源简介：
The inputs and scripts for MD simulations of the WT DNMT1 and its variants associated with autosomal dominant cerebellar ataxia–deafness and neuropathy (ADCA-DN) and hereditary sensory and autonomic neuropathy type 1E (HSAN1E).
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Zenodo创建时间：
2026-04-29
