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
The role of genetics in neurodegenerative dementia: a large cohort study in South China.
Jiao B et al.
Npj Genomic Medicine, 2021
34389718 (PubMed )
Supplement: 41525_2021_235_MOESM1_ESM.docx
Somatic TARDBP variants as a cause of semantic dementia.
van Rooij J et al.
Brain : a Journal of Neurology, 2020
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