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Author

G. Allington

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Review Aug 2026

De novo chromatin remodelling variants in sporadic Chiari 1 malformation.

Exome sequencing may complement surgical evaluation of children with sporadic CM1, particularly when accompanied by neurodevelopmental concerns, informing prognosis and family counseling, and implicating genetically encoded dysregulation of cerebellar development as a central disease mechanism.

Neel H. Mehta, Garrett Allington, Evan Dennis et al. · 0 citations

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