Published in
IOS Press, Journal of Alzheimer's Disease, 4(48), p. 923-926
DOI: 10.3233/jad-150477
Links
Tools
A Novel MAPT Mutation Causing Corticobasal Syndrome Led by Progressive Apraxia of Speech
Journal article published in 2015 by
Charles R. Marshall,
Rita Guerreiro,
Steffi Thust,
Phillip Fletcher,
Jonathan D. Rohrer,
Nick C. Fox 
This paper is available in a repository.
Full text: Download
Published version:
archiving forbidden
Data provided by 
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.