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Volumn 48, Issue , 2016, Pages 222.e9-222.e15

TYROBP genetic variants in early-onset Alzheimer's disease

(30)  Pottier, Cyril a   Ravenscroft, Thomas A a   Brown, Patricia H a   Finch, NiCole A a   Baker, Matt a   Parsons, Meeia a   Asmann, Yan W b   Ren, Yingxue a   Christopher, Elizabeth a   Levitch, Denise a   van Blitterswijk, Marka a   Cruchaga, Carlos c   Campion, Dominique d,e,f   Nicolas, Gaël d,e   Richard, Anne Claire d,e   Guerreiro, Rita g   Bras, Jose T g   Zuchner, Stephan h   Gonzalez, Michael A i   Bu, Guojun a   more..


Author keywords

Alzheimer's disease; Burden test; Exome sequencing; TREM2; TYROBP

Indexed keywords

ADULT; AGED; ALZHEIMER DISEASE; ARTICLE; CLINICAL ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; EARLY ONSET ALZHEIMER DISEASE; EXOME; FAMILY HISTORY; FEMALE; FOLLOW UP; GENE; GENE EXPRESSION; GENE IDENTIFICATION; GENE MUTATION; GENE OVEREXPRESSION; GENE SEQUENCE; GENETIC VARIABILITY; HUMAN; MALE; PATHOGENESIS; PILOT STUDY; PRIORITY JOURNAL; TREM2 GENE; TYROBP GENE; DOWN REGULATION; GENETIC ASSOCIATION STUDY; GENETIC VARIATION; GENETICS; HELA CELL LINE; METABOLISM; MIDDLE AGED; MUTATION; SEQUENCE ANALYSIS; VERY ELDERLY;

EID: 84994544504     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2016.07.028     Document Type: Article
Times cited : (76)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.