Exome sequencing identifies FUS mutations as a cause of essential tremor

American Journal of Human Genetics

Volumn 91, Issue 2, 2012, Pages 313-319

  Merner, Nancy D ^a,b   Girard, Simon L ^a,b   Catoire, Hélène ^a,b   Bourassa, Cynthia V ^a,b   Belzil, Véronique V ^a,b   Rivière, Jean Baptiste ^a,b   Hince, Pascale ^a,b   Levert, Annie ^a,b   Dionne Laporte, Alexandre ^a,b   Spiegelman, Dan ^a,b   Noreau, Anne ^a,b   Diab, Sabrina ^a,b   Szuto, Anna ^a,b   Fournier, Hélène ^c   Raelson, John ^c   Belouchi, Majid ^c   Panisset, Michel ^a,b   Cossette, Patrick ^a,b   Dupré, Nicolas ^d   Bernard, Geneviève ^a,b   Chouinard, Sylvain ^a,b   Dion, Patrick A ^a,b   Rouleau, Guy A ^a,b,e   more..

^a CENTRE HOSPITALIER DE L UNIVERSITÉ DE MONTRÉAL   (Canada)

^b UNIVERSITÉ DE MONTRÉAL   (Canada)

^c Genizon BioSciences Inc   (Canada)

^d UNIVERSITÉ LAVAL   (Canada)

^e UNIVERSITY OF MONTREAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

FUSED IN SARCOMA PROTEIN;

ADULT; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; ESSENTIAL TREMOR; EXOME; GENE MUTATION; GENE SEGREGATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

BASE SEQUENCE; ESSENTIAL TREMOR; EXOME; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MOLECULAR SEQUENCE DATA; POINT MUTATION; QUEBEC; RNA-BINDING PROTEIN FUS; SEQUENCE ANALYSIS, DNA;

EID: 84864931903     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2012.07.002     Document Type: Article

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