Screening UBQLN-2 in French frontotemporal lobar degeneration and frontotemporal lobar degeneration-amyotrophic lateral sclerosis patients

Neurobiology of Aging

Volumn 34, Issue 8, 2013, Pages 2078.e5-2078.e6

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

^a INSERM   (France)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c UNIVERSITÉ DE TOULOUSE   (France)

Author keywords

ALS; Frontotemporal lobar degeneration; FTLD; Ubiquilin; UBQLN 2

Indexed keywords

5' UNTRANSLATED REGION; AMYOTROPHIC LATERAL SCLEROSIS; ANG GENE; ARTICLE; C9ORF72 GENE; CHMP2B GENE; COHORT ANALYSIS; CONTROLLED STUDY; DISEASE ASSOCIATION; EXON; FRONTOTEMPORAL DEMENTIA; FUS TLS GENE; GENE; GENE MAPPING; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MAPT GENE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PFN1 GENE; PGRN GENE; PRIORITY JOURNAL; PROTEIN DOMAIN; SINGLE NUCLEOTIDE POLYMORPHISM; SOD1 GENE; TARDBP GENE; UBQLN 2 GENE; VCP GENE;

EID: 84877611002     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2013.03.002     Document Type: Article

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