ID   ND10666
AC   CVCL_BE75
DR   CLO; CLO_0034982
DR   Coriell; ND10666
DR   Wikidata; Q54923331
RX   PubMed=22572540;
CC   Sequence variation: Mutation; HGNC; HGNC:12666; VCP; Unexplicit; 3'UTR*12C>T; Zygosity=Heterozygous; Note=VUS (PubMed=22572540).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C34373; Amyotrophic lateral sclerosis
DI   ORDO; Orphanet_803; Amyotrophic lateral sclerosis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   47Y
CA   Transformed cell line
DT   Created: 02-05-16; Last updated: 19-12-24; Version: 10
//
RX   PubMed=22572540; DOI=10.1016/j.neurobiolaging.2012.04.005; PMCID=PMC3391327;
RA   Abramzon Y., Johnson J.O., Scholz S.W., Taylor J.P., Brunetti M.,
RA   Calvo A., Mandrioli J., Benatar M., Mora G., Restagno G., Chio A.,
RA   Traynor B.J.;
RT   "Valosin-containing protein (VCP) mutations in sporadic amyotrophic
RT   lateral sclerosis.";
RL   Neurobiol. Aging 33:2231.e1-2231.e6(2012).
//