Publication:
Pathogenic VCP (p.Arg453Trp) variant in three siblings with frontotemporal dementia-amyotrophic lateral sclerosis spectrum: a Turkish family

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dc.contributor.coauthorGültekin, Murat
dc.contributor.coauthorİlkhan, Beyzanur Altıkulaç
dc.contributor.coauthorBaydemir, Recep
dc.contributor.coauthorDeğirmenci, Yıldız
dc.contributor.departmentDepartment of Molecular Biology and Genetics
dc.contributor.kuauthorBaşak, Ayşe Nazlı
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.date.accessioned2026-07-02T07:31:00Z
dc.date.issued2026
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.versionPublished Version
dc.identifier.WoSQuartileQ2
dc.identifier.doi10.1016/j.clineuro.2026.109381
dc.identifier.eissn1872-6968
dc.identifier.embargoNo
dc.identifier.issn0303-8467
dc.identifier.pubmed41791136
dc.identifier.scopus2-s2.0-105035122093
dc.identifier.urihttps://doi.org/10.1016/j.clineuro.2026.109381
dc.identifier.urihttps://hdl.handle.net/20.500.14288/33084
dc.identifier.volume265
dc.identifier.wos001711438000001
dc.keywordsFrontotemporal dementia
dc.keywordsAmyotrophic lateral sclerosis
dc.keywordsVCP gene
dc.keywordsFTD-ALS spectrum
dc.keywordsGenetic mutation
dc.keywordsCase series
dc.languageeng
dc.publisherElsevier
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofClinical Neurology and Neurosurgery
dc.relation.openaccessN/A
dc.rightsN/A
dc.rights.uriN/A
dc.subjectClinical neurology
dc.subjectSurgery
dc.titlePathogenic VCP (p.Arg453Trp) variant in three siblings with frontotemporal dementia-amyotrophic lateral sclerosis spectrum: a Turkish family
dc.typeLetter
dspace.entity.typePublication
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