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Article

A Novel MAPT Mutation Causing Corticobasal Syndrome Led by Progressive Apraxia of Speech.

Journal of Alzheimer's disease : JAD - 1 Jan 2015

Marshall Charles R, Guerreiro Rita, Thust Steffi, Fletcher Phillip, Rohrer Jonathan D, Fox Nick C

Abstract excerpt

The authors describe a case of corticobasal syndrome led by progressive apraxia of speech, associated with a novel mutation in exon 10 of the MAPT gene. Genetic bases for progressive apraxia of speech and corticobasal syndrome are only rarely described, and have not been described in conjunction.

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Identifiers

PMID: 26402116
DOI: 10.3233/JAD-150477

Genes

MAPT

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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