Associated Papers
ANXA11 Mutations in the FTD Spectrum: A Novel Finding in a Patient With Semantic Variant Primary Progressive Aphasia.
Meng Y et al.
European Journal of Neurology, 2025
40345169 (PubMed )
Supplement: ENE-32-e70187-s001.docx
Nation-wide Japanese FTD consortium FTLD-J: Utility of case review meetings.
Sato S et al.
International Psychogeriatrics, 2025
A heterozygous splicing variant IVS9-7A > T in intron 9 of the MAPT gene in a patient with right-temporal variant frontotemporal dementia with atypical 4 repeat tauopathy.
Mori K et al.
Acta Neuropathologica Communications, 2023
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