Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France

Neurobiology of Aging

Volumn 34, Issue 6, 2013, Pages 1709.e1-1709.e2

  Lattante, Serena ^a   Le Ber, Isabelle ^a   Camuzat, Agnès ^a   Brice, Alexis ^a,b   Kabashi, Edor ^a  

^a INSTITUT DU CERVEAU ET DE LA MOELLE ÉPINIÈRE   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

Amyotrophic lateral sclerosis (ALS); Frontotemporal lobar degeneration (FTLD); PFN1

Indexed keywords

PROFILIN;

ADULT; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CONTROLLED STUDY; EXOME; FEMALE; FRANCE; FRONTOTEMPORAL DEMENTIA; GENE; GENE AMPLIFICATION; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; HUMAN; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; PFN GENE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

EID: 84875272260     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2012.10.026     Document Type: Article

References (0)