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Volumn 35, Issue 12, 2014, Pages 2881.e1-2881.e6

Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease

Author keywords

Alzheimer's disease; APP; Exome sequencing; GRN; MAPT; Neurodegenerative dementia; PRNP; PSEN1; PSEN2

Indexed keywords

AMYLOID PRECURSOR PROTEIN; APOLIPOPROTEIN E; PRESENILIN 1; PRESENILIN 2; APP PROTEIN, HUMAN; GRN PROTEIN, HUMAN; MAPT PROTEIN, HUMAN; PRION; PRNP PROTEIN, HUMAN; PSEN1 PROTEIN, HUMAN; PSEN2 PROTEIN, HUMAN; SIGNAL PEPTIDE; TAU PROTEIN;

EID: 84911430470     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2014.06.002     Document Type: Article
Times cited : (58)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.