Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients

Neurobiology of Aging

Volumn 35, Issue 12, 2014, Pages 2884.e1-2884.e4

  Chaussenot, Annabelle ^a,b   Le Ber, Isabelle ^c,d   Ait El Mkadem, Samira ^a,b   Camuzat, Agnès ^c   de Septenville, Anne ^c   Bannwarth, Sylvie ^a,b   Genin, Emmanuelle C ^a   Serre, Valérie ^e   Augé, Gaëlle ^a,b   Brice, Alexis ^c   Pouget, Jean ^f   Paquis Flucklinger, Véronique ^a,b  

^a UNIVERSITY OF NICE SOPHIA ANTIPOLIS   (France)

^b UNIVERSITY HOSPITAL OF NICE   (France)

^c SORBONNE UNIVERSITÉ   (France)

^d PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^e CNRS   (France)

^f TIMONE HOSPITAL   (France)

Author keywords

Amyotrophic lateral sclerosis (ALS); CHCHD10; Frontotemporal dementia (FTD); Frontotemporal lobar degeneration (FTLD); Mitochondrial disease

Indexed keywords

AGED; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; BULBAR PARALYSIS; CHCHD10 GENE; COHORT ANALYSIS; FRANCE; FRONTOTEMPORAL DEMENTIA; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE;

EID: 85027958118     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2014.07.022     Document Type: Article

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