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L266V MAPT Gene Mutation Associated With Frontotemporal Dementia, Progressive Supranuclear Palsy, and Corticobasal Syndrome

Rivas-Grajales AM, Han SC, Wang R, Greenstein P, Shih LC.

J Neuropsychiatry Clin Neurosci. 2025 Jan 10:appineuropsych20240128. doi: 10.1176/appi.neuropsych.20240128. Online ahead of print.

2025

PMID

39789940

PSP/CBD

L266V MAPT Gene Mutation Associated With Frontotemporal Dementia, Progressive Supranuclear Palsy, and Corticobasal Syndrome
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