Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosis

Neurobiology of Aging

Volumn 33, Issue 9, 2012, Pages 2231.e1-2231.e6

  Abramzon, Yevgeniya ^a   Johnson, Janel O ^a   Scholz, Sonja W ^a,b   Taylor, J P ^c   Brunetti, Maura ^d   Calvo, Andrea ^e   Mandrioli, Jessica ^f   Benatar, Michael ^g   Mora, Gabriele ^h   Restagno, Gabriella ^d   Chiò, Adriano ^e   Traynor, Bryan J ^a,i  

^a NATIONAL INSTITUTE ON AGING   (United States)

^b GEORGETOWN UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

^d ASO OIRM S Anna   (Italy)

^e UNIVERSITY OF TURIN   (Italy)

^f UNIVERSITY OF MODENA AND REGGIO EMILIA   (Italy)

^g UNIVERSITY OF MIAMI MILLER SCHOOL OF MEDICINE   (United States)

^h IRCCS   (Italy)

ⁱ JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Amyotrophic lateral sclerosis; Mutations; Sporadic disease; Valosin containing protein

Indexed keywords

VALOSIN CONTAINING PROTEIN;

AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CONTROLLED STUDY; GENE FUNCTION; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MOTOR NEUROPATHY; MUTATIONAL ANALYSIS; MUTATOR GENE; PATHOPHYSIOLOGY; PRIORITY JOURNAL; SEQUENCE ANALYSIS; UNITED STATES; VALOSIN CONTAINING PROTEIN GENE;

EID: 84863443830     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2012.04.005     Document Type: Article

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