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Volumn 36, Issue 11, 2015, Pages 3116.e5-3116.e8

TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts

(27)  Le Ber, Isabelle a,b   De Septenville, Anne a   Millecamps, Stéphanie a   Camuzat, Agnès a   Caroppo, Paola a,c   Couratier, Philippe d   Blanc, Frédéric e,k   Lacomblez, Lucette b,f   Sellal, François g,h,i,t   Fleury, Marie Céline e   Meininger, Vincent b   Cazeneuve, Cécile b   Clot, Fabienne b   Flabeau, Olivier j   LeGuern, Eric a,b   Brice, Alexis a,b   Didic, Mira l   Dubois, Bruno b   Golfier, Véronique m   Hannequin, Didier n   more..

f INSERM   (France)

Author keywords

Amyotrophic lateral sclerosis (ALS); Frontotemporal dementia (FTD); Frontotemporal lobar degeneration (FTLD); Loss of function; Optineurin; TBK1

Indexed keywords

ADULT; AGED; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; C9ORF72 GENE; COHORT ANALYSIS; CONTROLLED STUDY; FRENCHMAN; FRONTOTEMPORAL DEMENTIA; GENE; GENE SEQUENCE; HETEROZYGOTE; HUMAN; LOSS OF FUNCTION MUTATION; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MUTATION RATE; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; TBK1 GENE; FRANCE; GENETIC ASSOCIATION STUDY; GENETICS; MUTATION;

EID: 84946431031     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2015.08.009     Document Type: Article
Times cited : (71)

References (11)
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    • Weidberg, H.1    Elazar, Z.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.