The progranulin (GRN) Cys157LysfsX97 mutation is associated with nonfluent variant of primary progressive aphasia clinical phenotype

Journal of Alzheimer's Disease

Volumn 28, Issue 4, 2012, Pages 759-763

  Caso, Francesca ^a   Villa, Chiara ^b   Fenoglio, Chiara ^b   Santangelo, Roberto ^a   Agosta, Federica ^a   Coppi, Elisabetta ^a   Falautano, Monica ^a   Comi, Giancarlo ^a   Filippi, Massimo ^a   Scarpini, Elio ^b   Magnani, Giuseppe ^a   Galimberti, Daniela ^b  

^a VITA SALUTE SAN RAFFAELE UNIVERSITY   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

Author keywords

Alzheimer's disease; Dementia; frontotemporal lobar degeneration; GRN mutation; nonfluent variant of primary progressive aphasia; progranulin

Indexed keywords

DNA; FLUORODEOXYGLUCOSE F 18; PROGRANULIN;

ADULT; ANXIETY DISORDER; APHASIA; ARTICLE; CASE REPORT; CLINICAL DEMENTIA RATING; COGNITIVE DEFECT; COMPREHENSION; DAILY LIFE ACTIVITY; DISEASE COURSE; DNA EXTRACTION; DNA SEQUENCE; FEMALE; FOLLOW UP; FRONTOTEMPORAL DEMENTIA; GENE MUTATION; GENETIC ASSOCIATION; GENOTYPE; HUMAN; INSOMNIA; MAJOR DEPRESSION; MINI MENTAL STATE EXAMINATION; NEUROIMAGING; NEUROPSYCHOLOGY; NONFLUENT VARIANT PRIMARY PROGRESSIVE APHASIA; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PANIC; PHENOTYPE; PHONEME; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL; RATING SCALE; STRUCTURED INTERVIEW;

EID: 84858055987     PISSN: 13872877     EISSN: 18758908     Source Type: Journal    
DOI: 10.3233/JAD-2011-111544     Document Type: Article

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