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Illustration of a rare case of hereditary spastic paraplegia type 30 associated with a missense variant in the non‑motor domain of KIF1A

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dc.contributor.coauthorOnder, Halil
dc.contributor.coauthorDuzkale, Neslihan
dc.contributor.coauthorKocer, Bilge
dc.contributor.coauthorComoglu, Selcuk
dc.contributor.departmentKUH (Koç University Hospital)
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorVural, Atay
dc.contributor.schoolcollegeinstituteKUH (KOÇ UNIVERSITY HOSPITAL)
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:09:31Z
dc.date.issued2022
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue6
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume269
dc.identifier.doi10.1007/s00415-021-10924-9
dc.identifier.eissn1432-1459
dc.identifier.issn0340-5354
dc.identifier.scopus2-s2.0-85122663437
dc.identifier.urihttps://doi.org/10.1007/s00415-021-10924-9
dc.identifier.urihttps://hdl.handle.net/20.500.14288/9318
dc.identifier.wos740397400001
dc.keywordsMotor domain
dc.keywordsMutations
dc.keywordsNeuropathy
dc.keywordsSPG30
dc.language.isoeng
dc.publisherSpringer Heidelberg
dc.relation.ispartofJournal of Neurology
dc.subjectClinical neuropsychology
dc.titleIllustration of a rare case of hereditary spastic paraplegia type 30 associated with a missense variant in the non‑motor domain of KIF1A
dc.typeLetter
dspace.entity.typePublication
local.contributor.kuauthorVural, Atay
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit1KUH (KOÇ UNIVERSITY HOSPITAL)
local.publication.orgunit2KUH (Koç University Hospital)
local.publication.orgunit2School of Medicine
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