Associated Papers
Dissecting the Clinical Heterogeneity and Genotype-Phenotype Correlations of MAPT Mutations: A Systematic Review.
Villa C et al.
Frontiers in Bioscience (landmark Edition), 2024
A novel MAPT variant (E342K) as a cause of familial progressive supranuclear palsy.
Li H et al.
Frontiers in Neurology, 2024
Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features.
Rossi G et al.
Neurobiology of Aging, 2014
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