Unravelling Genetic Factors Underlying Corticobasal Syndrome: A Systematic Review.

Cells · 2021 · PMC7830591 · PMID 33467748

Europe PMC DOI

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did not reach statistical significanceno p-value reported

Apraxia, myoclonus, and visuospatial impairment seem more frequent in this group, but this finding did not reach statistical significance, probably because of the small sample size.

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