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

Abstract

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.

Keywords

Corticobasal syndrome frontotemporal dementia microtubule-associated protein tau progressive apraxia of speech

Get full access to this article

View all access options for this article.

References

10.

11.

12.

13.

14.

15.