{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T13:31:38Z","timestamp":1791207098508,"version":"4.1.0"},"reference-count":60,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2013,4,1]],"date-time":"2013-04-01T00:00:00Z","timestamp":1364774400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"crossref","award":["30971002"],"award-info":[{"award-number":["30971002"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"crossref"}]},{"name":"International Cooperation and Exchange National Natural Science Foundation of China","award":["30911120496"],"award-info":[{"award-number":["30911120496"]}]},{"name":"Innovation Fund of Chinese Academy of Medical Sciences and Peking Union Medical College","award":["X2010020"],"award-info":[{"award-number":["X2010020"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Neurobiology of Aging"],"published-print":{"date-parts":[[2013,4]]},"DOI":"10.1016\/j.neurobiolaging.2012.09.005","type":"journal-article","created":{"date-parts":[[2012,10,6]],"date-time":"2012-10-06T22:00:36Z","timestamp":1349560836000},"page":"1312.e1-1312.e8","source":"Crossref","is-referenced-by-count":61,"title":["De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China"],"prefix":"10.1016","volume":"34","author":[{"given":"Zhang-Yu","family":"Zou","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Li-Ying","family":"Cui","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Qing","family":"Sun","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiao-Guang","family":"Li","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ming-Sheng","family":"Liu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yan","family":"Xu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yan","family":"Zhou","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xun-Zhe","family":"Yang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib1","doi-asserted-by":"crossref","first-page":"680","DOI":"10.1002\/ana.10369","article-title":"\u201cTrue\u201d sporadic ALS associated with a novel SOD-1 mutation","volume":"52","author":"Alexander","year":"2002","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib2","doi-asserted-by":"crossref","first-page":"603","DOI":"10.1038\/nrneurol.2011.150","article-title":"Clinical genetics of amyotrophic lateral sclerosis: what do we really know?","volume":"7","author":"Andersen","year":"2011","journal-title":"Nat. Rev. Neurol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib3","doi-asserted-by":"crossref","first-page":"611","DOI":"10.1212\/WNL.0b013e3181ed9cde","article-title":"Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations","volume":"75","author":"Baumer","year":"2010","journal-title":"Neurology"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib4","doi-asserted-by":"crossref","first-page":"113","DOI":"10.3109\/17482968.2010.536840","article-title":"Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis","volume":"12","author":"Belzil","year":"2011","journal-title":"Amyotroph. Lateral Scler."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib5","article-title":"Novel FUS deletion in a patient with juvenile amyotrophic lateral sclerosis [e-pub ahead of print]","author":"Belzil","year":"2012","journal-title":"Arch. Neurol"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib6","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1038\/jhg.2010.162","article-title":"Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis","volume":"56","author":"Belzil","year":"2011","journal-title":"J.\u00a0Hum. Genet."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib7","doi-asserted-by":"crossref","first-page":"1176","DOI":"10.1212\/WNL.0b013e3181bbfeef","article-title":"Mutations in FUS cause FALS and SALS in French and French Canadian populations","volume":"73","author":"Belzil","year":"2009","journal-title":"Neurology"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib8","doi-asserted-by":"crossref","first-page":"639","DOI":"10.1136\/jnnp.2009.194399","article-title":"FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis","volume":"81","author":"Blair","year":"2010","journal-title":"J.\u00a0Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib9","doi-asserted-by":"crossref","first-page":"4160","DOI":"10.1093\/hmg\/ddq335","article-title":"Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules","volume":"19","author":"Bosco","year":"2010","journal-title":"Hum. Mol. Genet."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib10","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1080\/146608200300079536","article-title":"El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis","volume":"1","author":"Brooks","year":"2000","journal-title":"Amyotroph. Lateral Scler. Other Motor Neuron Disord."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib11","doi-asserted-by":"crossref","first-page":"765","DOI":"10.3233\/JAD-2010-100837","article-title":"FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis","volume":"22","author":"Broustal","year":"2010","journal-title":"J.\u00a0Alzheimers Dis."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib12","doi-asserted-by":"crossref","first-page":"217","DOI":"10.3109\/17482968.2011.643899","article-title":"SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: a United States clinical testing lab experience","volume":"13","author":"Brown","year":"2012","journal-title":"Amyotroph. Lateral Scler."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib13","doi-asserted-by":"crossref","first-page":"157","DOI":"10.3109\/17482968.2010.545420","article-title":"Proposed criteria for familial amyotrophic lateral sclerosis","volume":"12","author":"Byrne","year":"2011","journal-title":"Amyotroph. Lateral Scler."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib14","doi-asserted-by":"crossref","first-page":"1128","DOI":"10.1086\/421054","article-title":"DNA\/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)","volume":"74","author":"Chen","year":"2004","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib15","doi-asserted-by":"crossref","first-page":"e523","DOI":"10.1016\/j.neurobiolaging.2010.05.016","article-title":"A\u00a0de novo missense mutation of the FUS gene in a \u201ctrue\u201d sporadic ALS case","volume":"32","author":"Chio","year":"2011","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib16","doi-asserted-by":"crossref","first-page":"1272","DOI":"10.1016\/j.neurobiolaging.2009.05.001","article-title":"Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation","volume":"30","author":"Chio","year":"2009","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib17","doi-asserted-by":"crossref","first-page":"533","DOI":"10.1212\/01.wnl.0000299187.90432.3f","article-title":"Prevalence of SOD1 mutations in the Italian ALS population","volume":"70","author":"Chio","year":"2008","journal-title":"Neurology"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib18","doi-asserted-by":"crossref","first-page":"73","DOI":"10.1016\/j.nmd.2011.08.003","article-title":"P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis","volume":"22","author":"Conte","year":"2012","journal-title":"Neuromuscul. Disord."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib19","doi-asserted-by":"crossref","first-page":"190","DOI":"10.1136\/jmg.2009.071027","article-title":"Mutations of FUS gene in sporadic amyotrophic lateral sclerosis","volume":"47","author":"Corrado","year":"2010","journal-title":"J.\u00a0Med. Genet."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib20","doi-asserted-by":"crossref","first-page":"754","DOI":"10.1111\/j.1468-1331.2009.02859.x","article-title":"The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALS","volume":"17","author":"Damme","year":"2010","journal-title":"Eur. J. Neurol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib21","doi-asserted-by":"crossref","first-page":"E1377","DOI":"10.1002\/humu.21241","article-title":"De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis","volume":"31","author":"DeJesus-Hernandez","year":"2010","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib22","doi-asserted-by":"crossref","first-page":"2841","DOI":"10.1038\/emboj.2010.143","article-title":"ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import","volume":"29","author":"Dormann","year":"2010","journal-title":"EMBO J."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib23","doi-asserted-by":"crossref","first-page":"e541","DOI":"10.1016\/j.neurobiolaging.2009.11.017","article-title":"C-terminal FUS\/TLS mutations in familial and sporadic ALS in Germany","volume":"32","author":"Drepper","year":"2011","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib24","doi-asserted-by":"crossref","first-page":"663","DOI":"10.1007\/s12031-011-9637-9","article-title":"Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia","volume":"45","author":"Fecto","year":"2011","journal-title":"J.\u00a0Mol. Neurosci."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib25","doi-asserted-by":"crossref","first-page":"323","DOI":"10.1080\/17482960701553956","article-title":"Young-onset sporadic amyotrophic lateral sclerosis: a distinct nosological entity?","volume":"8","author":"Gouveia","year":"2007","journal-title":"Amyotroph. Lateral Scler."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib26","doi-asserted-by":"crossref","first-page":"224","DOI":"10.1001\/archneurol.2009.329","article-title":"FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands","volume":"67","author":"Groen","year":"2010","journal-title":"Arch. Neurol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib27","doi-asserted-by":"crossref","first-page":"166","DOI":"10.1038\/ng1001-166","article-title":"A\u00a0gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2","volume":"29","author":"Hadano","year":"2001","journal-title":"Nat. Genet."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib28","doi-asserted-by":"crossref","first-page":"174","DOI":"10.1136\/jmg.35.2.174","article-title":"Homozygosity for Asn86Ser mutation in the CuZn-superoxide dismutase gene produces a severe clinical phenotype in a juvenile onset case of familial amyotrophic lateral sclerosis","volume":"35","author":"Hayward","year":"1998","journal-title":"J.\u00a0Med. Genet."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib29","doi-asserted-by":"crossref","first-page":"455","DOI":"10.1001\/archneurol.2010.52","article-title":"Novel FUS\/TLS mutations and pathology in familial and sporadic amyotrophic lateral sclerosis","volume":"67","author":"Hewitt","year":"2010","journal-title":"Arch. Neurol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib30","doi-asserted-by":"crossref","first-page":"1069","DOI":"10.1111\/j.1750-3639.2010.00413.x","article-title":"Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusions","volume":"20","author":"Huang","year":"2010","journal-title":"Brain Pathol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib31","doi-asserted-by":"crossref","first-page":"152","DOI":"10.1002\/ana.22246","article-title":"Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS\/TLS","volume":"69","author":"Ito","year":"2011","journal-title":"Ann. Neurol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib32","doi-asserted-by":"crossref","first-page":"555","DOI":"10.1007\/s00401-011-0809-z","article-title":"Optineurin is co-localized with FUS in basophilic inclusions of ALS with FUS mutation and in basophilic inclusion body disease","volume":"121","author":"Ito","year":"2011","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib33","doi-asserted-by":"crossref","first-page":"356","DOI":"10.1002\/(SICI)1098-1004(1997)9:4<356::AID-HUMU9>3.0.CO;2-3","article-title":"Novel G16S (GGC-AGC) mutation in the SOD-1 gene in a patient with apparently sporadic young-onset amyotrophic lateral sclerosis","volume":"9","author":"Kawamata","year":"1997","journal-title":"Hum. Mutat."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib34","doi-asserted-by":"crossref","first-page":"237","DOI":"10.3109\/17482968.2011.627588","article-title":"A\u00a0novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression","volume":"13","author":"Keckarevic","year":"2012","journal-title":"Amyotroph. Lateral Scler."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib35","doi-asserted-by":"crossref","first-page":"942","DOI":"10.1016\/S0140-6736(10)61156-7","article-title":"Amyotrophic lateral sclerosis","volume":"377","author":"Kiernan","year":"2011","journal-title":"Lancet"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib36","doi-asserted-by":"crossref","first-page":"1205","DOI":"10.1126\/science.1166066","article-title":"Mutations in the FUS\/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis","volume":"323","author":"Kwiatkowski","year":"2009","journal-title":"Science"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib37","doi-asserted-by":"crossref","first-page":"e1017","DOI":"10.1016\/j.neurobiolaging.2011.12.003","article-title":"Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS","volume":"33","author":"Kwon","year":"2012","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib38","doi-asserted-by":"crossref","first-page":"e551","DOI":"10.1016\/j.neurobiolaging.2009.12.020","article-title":"FUS mutations in sporadic amyotrophic lateral sclerosis","volume":"32","author":"Lai","year":"2011","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib39","doi-asserted-by":"crossref","first-page":"385","DOI":"10.1136\/jnnp.2009.183525","article-title":"Incidence of amyotrophic lateral sclerosis in Europe","volume":"81","author":"Logroscino","year":"2010","journal-title":"J.\u00a0Neurol. Neurosurg. Psychiatry"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib40","doi-asserted-by":"crossref","first-page":"995","DOI":"10.1016\/S1474-4422(10)70195-2","article-title":"TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia","volume":"9","author":"Mackenzie","year":"2010","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib41","doi-asserted-by":"crossref","first-page":"554","DOI":"10.1136\/jmg.2010.077180","article-title":"SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations","volume":"47","author":"Millecamps","year":"2010","journal-title":"J.\u00a0Med. Genet."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib42","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1016\/S0072-9752(07)80018-2","article-title":"Chapter 15 Juvenile amyotrophic lateral sclerosis","volume":"82","author":"Orban","year":"2007","journal-title":"Handb. Clin. Neurol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib43","doi-asserted-by":"crossref","first-page":"591","DOI":"10.1093\/brain\/awp325","article-title":"SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis","volume":"133","author":"Orlacchio","year":"2010","journal-title":"Brain"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib44","doi-asserted-by":"crossref","first-page":"170","DOI":"10.1002\/mus.21665","article-title":"Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis","volume":"42","author":"Rademakers","year":"2010","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib45","doi-asserted-by":"crossref","first-page":"162","DOI":"10.1080\/aml.4.3.162.166","article-title":"A\u00a0rare Cu\/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset, incomplete penetrance and a sensory neuropathy","volume":"4","author":"Rezania","year":"2003","journal-title":"Amyotroph. Lateral Scler. Other Motor Neuron Disord."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib46","doi-asserted-by":"crossref","first-page":"e527","DOI":"10.1016\/j.neurobiolaging.2010.05.015","article-title":"A\u00a0novel double mutation in FUS gene causing sporadic ALS","volume":"32","author":"Robertson","year":"2011","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib47","doi-asserted-by":"crossref","first-page":"e423","DOI":"10.1016\/j.neurobiolaging.2010.09.029","article-title":"Pathogenicity of exonic indels in fused in sarcoma in amyotrophic lateral sclerosis","volume":"33","author":"Rutherford","year":"2012","journal-title":"Neurobiol Aging."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib48","doi-asserted-by":"crossref","first-page":"e831","DOI":"10.1016\/j.neurobiolaging.2011.10.005","article-title":"FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis","volume":"33","author":"Sproviero","year":"2012","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib49","doi-asserted-by":"crossref","first-page":"252","DOI":"10.1038\/jhg.2010.16","article-title":"FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion","volume":"55","author":"Suzuki","year":"2010","journal-title":"J.\u00a0Hum. Genet."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib50","doi-asserted-by":"crossref","first-page":"118","DOI":"10.3109\/17482968.2010.539235","article-title":"FUS\/TLS gene mutations are the second most frequent cause of familial ALS in the Spanish population","volume":"12","author":"Syriani","year":"2011","journal-title":"Amyotroph. Lateral Scler."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib51","doi-asserted-by":"crossref","first-page":"355","DOI":"10.1007\/s00401-009-0621-1","article-title":"Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation","volume":"119","author":"Tateishi","year":"2010","journal-title":"Acta Neuropathol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib52","doi-asserted-by":"crossref","first-page":"1180","DOI":"10.1212\/WNL.0b013e3181bbff05","article-title":"Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort","volume":"73","author":"Ticozzi","year":"2009","journal-title":"Neurology"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib53","doi-asserted-by":"crossref","first-page":"553.e513","DOI":"10.1016\/j.neurobiolaging.2010.04.009","article-title":"FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS","volume":"32","author":"Tsai","year":"2011","journal-title":"Neurobiol. Aging"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib54","doi-asserted-by":"crossref","first-page":"1208","DOI":"10.1126\/science.1165942","article-title":"Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6","volume":"323","author":"Vance","year":"2009","journal-title":"Science"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib55","doi-asserted-by":"crossref","first-page":"815","DOI":"10.1212\/WNL.0b013e3181f07e26","article-title":"Novel missense and truncating mutations in FUS\/TLS in familial ALS","volume":"75","author":"Waibel","year":"2010","journal-title":"Neurology"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib56","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1016\/j.jns.2010.06.008","article-title":"A\u00a0Japanese ALS6 family with mutation R521C in the FUS\/TLS gene: a clinical, pathological and genetic report","volume":"296","author":"Yamamoto-Watanabe","year":"2010","journal-title":"J.\u00a0Neurol. Sci."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib57","first-page":"1039","article-title":"Sporadic juvenile amyotrophic lateral sclerosis caused by mutant FUS\/TLS: possible association of mental retardation with this mutation","volume":"259","author":"Yamashita","year":"2011","journal-title":"J.\u00a0Neurol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib58","doi-asserted-by":"crossref","first-page":"807","DOI":"10.1212\/WNL.0b013e3181f07e0c","article-title":"Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS\/dementia","volume":"75","author":"Yan","year":"2010","journal-title":"Neurology"},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib59","doi-asserted-by":"crossref","first-page":"977","DOI":"10.1111\/j.1468-1331.2012.03662.x","article-title":"Screening of the FUS gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin","volume":"19","author":"Zou","year":"2012","journal-title":"Eur. J. Neurol."},{"key":"10.1016\/j.neurobiolaging.2012.09.005_bib60","doi-asserted-by":"crossref","first-page":"2229.e11","DOI":"10.1016\/j.neurobiolaging.2012.03.014","article-title":"Screening of the TARDBP gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin","volume":"33","author":"Zou","year":"2012","journal-title":"Neurobiol. Aging"}],"container-title":["Neurobiology of Aging"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0197458012004617?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0197458012004617?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,4,10]],"date-time":"2025-04-10T02:59:39Z","timestamp":1744253979000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0197458012004617"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,4]]},"references-count":60,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2013,4]]}},"alternative-id":["S0197458012004617"],"URL":"https:\/\/doi.org\/10.1016\/j.neurobiolaging.2012.09.005","relation":{},"ISSN":["0197-4580"],"issn-type":[{"value":"0197-4580","type":"print"}],"subject":[],"published":{"date-parts":[[2013,4]]}}}