Novel missense progranulin gene mutation associated with the semantic variant of primary progressive aphasia

Journal of Alzheimer's Disease

Volumn 36, Issue 3, 2013, Pages 415-420

  Cerami, Chiara ^a   Marcone, Alessandra ^a   Galimberti, Daniela ^b   Villa, Chiara ^b   Fenoglio, Chiara ^b   Scarpini, Elio ^b   Cappa, Stefano F ^a  

^a VITA SALUTE SAN RAFFAELE UNIVERSITY   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

Author keywords

Frontotemporal lobar degeneration; GRN mutation; semantic variant of primary progressive aphasia

Indexed keywords

FLUORODEOXYGLUCOSE F 18; PROGRANULIN;

ADULT; ANOMIA; ARTICLE; BRAIN ATROPHY; BRAIN METABOLISM; CASE REPORT; CONTRAST ENHANCEMENT; CONTROLLED STUDY; DEMENTIA; EXON; FAMILY HISTORY; FOLLOW UP; GENETIC ASSOCIATION; GENETIC CONSERVATION; HUMAN; MALE; MINI MENTAL STATE EXAMINATION; MISSENSE MUTATION; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; POSITRON EMISSION TOMOGRAPHY; PRIMARY PROGRESSIVE APHASIA; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN STRUCTURE; PSYCHOLOGIC ASSESSMENT; SEMANTIC VARIANT PRIMARY PROGRESSIVE APHASIA;

EID: 84881436989     PISSN: 13872877     EISSN: 18758908     Source Type: Journal    
DOI: 10.3233/JAD-130317     Document Type: Article

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