Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis

Neurobiology of Aging

Volumn 33, Issue 3, 2012, Pages 630.e1-630.e2

  Tiloca, Cinzia ^a   Ratti, Antonia ^a,b   Pensato, Viviana ^c   Castucci, Alessia ^c   Sorarù, Gianni ^d   Del Bo, Roberto ^b,e   Corrado, Lucia ^f   Cereda, Cristina ^g   D'Ascenzo, Carla ^d   Comi, Giacomo P ^b,e   Mazzini, Letizia ^f   Castellotti, Barbara ^c   Ticozzi, Nicola ^a   Gellera, Cinzia ^c   Silani, Vincenzo ^a,b  

^a ISTITUTO AUXOLOGICO ITALIANO   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

^c DEPARTMENT OF NEUROSURGERY   (Italy)

^d UNIVERSITY OF PADOVA   (Italy)

^e FONDAZIONE IRCCS CA GRANDA OSPEDALE MAGGIORE POLICLINICO   (Italy)

^f UNIVERSITY OF EASTERN PIEDMONT   (Italy)

^g C MONDINO NATIONAL NEUROLOGICAL INSTITUTE   (Italy)

Author keywords

ALS (Amyotrophic lateral sclerosis); Genetics; VCP (valosin containing protein)

Indexed keywords

VALOSIN CONTAINING PROTEIN;

3' UNTRANSLATED REGION; AMYOTROPHIC LATERAL SCLEROSIS; AMYOTROPHIC LATERAL SCLEROSIS FRONTOTEMPORAL DEMENTIA; ARTICLE; BIOINFORMATICS; COHORT ANALYSIS; FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS; GENE; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; ITALY; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; RNA SPLICING; VCP GENE;

EID: 84855809916     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2011.10.025     Document Type: Article

References (1)

1. Johnson J.O., Mandrioli J., Benatar M., Abramzon Y., Van Deerlin V.M., Trojanowski J.Q., Gibbs J.R., Brunetti M., Gronka S., Wuu J., Ding J., McCluskey L., Martinez-Lage M., Falcone D., Hernandez D.G., Arepalli S., Chong S., Schymick J.C., Rothstein J., Landi F., Wang Y.D., Calvo A., Mora G., Sabatelli M., Monsurrò M.R., Battistini S., Salvi F., Spataro R., Sola P., Borghero G., Galassi G., Scholz S.W., Taylor J.P., Restagno G., Chiò A., Traynor B.J. Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron 2010, 68:857-864. ITALSGEN Consortium.