Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patients

Neurobiology of Aging

Volumn 34, Issue 4, 2013, Pages 1311.e1-1311.e2

  Daoud, Hussein ^a   Dobrzeniecka, Sylvia ^a   Camu, William ^b   Meininger, Vincent ^c   Dupré, Nicolas ^d   Dion, Patrick A ^a,e   Rouleau, Guy A ^a,f  

^a UNIVERSITY OF MONTREAL   (Canada)

^b MONTPELLIER UNIVERSITY HOSPITAL   (France)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^d UNIVERSITÉ LAVAL   (Canada)

^e UNIVERSITÉ DE MONTRÉAL   (Canada)

^f UNIVERSITY OF MONTREAL   (Canada)

Author keywords

Familial ALS; Mutation analysis; PFN1

Indexed keywords

AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; C9ORF72 GENE; CAUCASIAN; FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS; FUS GENE; GENE; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; HUMAN; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PFN1 GENE; PREVALENCE; PRIORITY JOURNAL; PROMOTER REGION; SEQUENCE ANALYSIS; SOD1 GENE; TARDBP GENE;

EID: 84872346600     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2012.09.001     Document Type: Article

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