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 new MAPT deletion in a case of speech apraxia leading to corticobasal syndrome.
Mazzon G et al.
Neurocase, 2018
A Novel MAPT Mutation Causing Corticobasal Syndrome Led by Progressive Apraxia of Speech.
Marshall CR et al.
Journal of Alzheimer's Disease : Jad, 2015
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