A novel MAPT mutation causing corticobasal syndrome led by progressive apraxia of speech

Journal of Alzheimer's Disease

Volumn 48, Issue 4, 2015, Pages 923-926

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

^a Department of Neurodegenerative Disease ^*  (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

Author keywords

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

Indexed keywords

ADULT; APRAXIA OF SPEECH; ARTICLE; BRAIN ATROPHY; CASE REPORT; CORTICOBASAL DEGENERATION; DISEASE SEVERITY; EXON; FEMALE; GENE; GENE MUTATION; HETEROZYGOSITY; HUMAN; INFERIOR FRONTAL GYRUS; MAPT GENE; MIDDLE AGED; NEUROPSYCHOLOGICAL TEST; NEXT GENERATION SEQUENCING; NUCLEAR MAGNETIC RESONANCE IMAGING; PRECENTRAL SULCUS; PREMOTOR CORTEX; PRIMARY MOTOR CORTEX; PRIORITY JOURNAL; APRAXIAS; ATROPHY; BRAIN; DIFFERENTIAL DIAGNOSIS; GENETICS; MUTATION; NEURODEGENERATIVE DISEASES; PATHOLOGY; PATHOPHYSIOLOGY; SEQUENCE ANALYSIS; SPEECH;

MAPT PROTEIN, HUMAN; TAU PROTEIN;

APRAXIAS; ATROPHY; BRAIN; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MIDDLE AGED; MUTATION; NEURODEGENERATIVE DISEASES; NEUROPSYCHOLOGICAL TESTS; SEQUENCE ANALYSIS; SPEECH; TAU PROTEINS;

EID: 84946059849     PISSN: 13872877     EISSN: 18758908     Source Type: Journal    
DOI: 10.3233/JAD-150477     Document Type: Article

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