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Predicting high-risk clinical missense variants of SMARCB1 in rare neurogenetic disorder schwannomatosis (nerve tumor) through sequence, structure, and molecular dynamics analyses

Crossref DOI link: https://doi.org/10.1007/s10048-025-00812-z

Published Online: 2025-02-20

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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