FUS and TDP43 genetic variability in FTD and CBS

Neurobiology of Aging

Volumn 33, Issue 5, 2012, Pages 1016.e9-1016.e17

  Huey, Edward D ^a,b   Ferrari, Raffaele ^c,d   Moreno, Jorge H ^c   Jensen, Christopher ^c   Morris, Christopher M ^e   Potocnik, Felix ^f   Kalaria, Rajesh N ^e   Tierney, Michael ^b   Wassermann, Eric M ^b   Hardy, John ^d,g   Grafman, Jordan ^b,h   Momeni, Parastoo ^c  

^a Taub Institute for Research on Alzheimer's Disease and the Aging Brain and the Gertrude H Sergievsky Center   (United States)

^b NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE   (United States)

^c TEXAS TECH UNIVERSITY HEALTH SCIENCES CENTER SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

^e NEWCASTLE UNIVERSITY   (United Kingdom)

^f STELLENBOSCH UNIVERSITY   (South Africa)

^g NATIONAL INSTITUTE ON AGING   (United States)

^h KESSLER FOUNDATION   (United States)

Author keywords

Corticobasal syndrome; Frontotemporal dementia; FUS; Genetics; TDP 43

Indexed keywords

ADULT; AGED; ARTICLE; BRAIN DISEASE; CONTROLLED STUDY; CORTICOBASAL SYNDROME; EXON; FEMALE; FRONTOTEMPORAL DEMENTIA; FUS GENE; GENE; GENE DELETION; GENE INSERTION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; HETEROZYGOSITY; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; TDP43 GENE;

EID: 84858334126     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2011.08.004     Document Type: Article

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