Publication:
Correction to: clinical, electrophysiological, and genetic analysis of a family with two rare neuromuscular disorders: congenital myasthenic syndrome and hereditary polyneuropathy

Simple item page
dc.contributor.coauthorTezen, Didem
dc.contributor.coauthorGündüz, Ayşegül
dc.contributor.coauthorDeymeer, Feza
dc.contributor.coauthorDemirbilek, Veysi
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.departmentNDAL (Neurodegeneration Research Laboratory)
dc.contributor.departmentSchool of Medicine
dc.contributor.facultymemberYes
dc.contributor.kuauthorKhojakulov, Zakhiriddin
dc.contributor.kuauthorBaşak, Ayşe Nazlı
dc.contributor.schoolcollegeinstituteLaboratory
dc.contributor.schoolcollegeinstituteResearch Center
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-03-06T20:59:36Z
dc.date.issued2024
dc.description.abstractThe original version of this article contains an error in the author’s affiliation. Feza Deymeer should be affiliated only with affiliation 3, and affiliation 1 should be removed from Feza Deymeer’s address. The original article has been corrected.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessN/A
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.WoSQuartileQ3
dc.identifier.doi10.1007/s10072-024-07805-0
dc.identifier.eissn1590-3478
dc.identifier.embargoN/A
dc.identifier.endpage5991
dc.identifier.issn1590-1874
dc.identifier.issue12
dc.identifier.pubmed39387956
dc.identifier.scopus2-s2.0-85206385757
dc.identifier.startpage5991
dc.identifier.urihttps://doi.org/10.1007/s10072-024-07805-0
dc.identifier.urihttps://hdl.handle.net/20.500.14288/27749
dc.identifier.volume45
dc.identifier.wos001336737800002
dc.keywordsCongenital myasthenic syndrome
dc.keywordsHereditary polyneuropathy
dc.keywordsNeuromuscular disorders
dc.keywordsRare diseases
dc.keywordsElectrophysiology
dc.keywordsGenetic analysis
dc.keywordsFamily study
dc.keywordsInherited neuropathy
dc.keywordsNeuromuscular junction
dc.keywordsNeurogenetics
dc.keywordsCorrection
dc.language.isoeng
dc.publisherSpringer
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofNeurological Sciences
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectClinical neurology
dc.subjectNeurogenetics
dc.subjectMedical genetics
dc.titleCorrection to: clinical, electrophysiological, and genetic analysis of a family with two rare neuromuscular disorders: congenital myasthenic syndrome and hereditary polyneuropathy
dc.typeOther
dspace.entity.typePublication
local.contributor.kuauthorBaşak, Ayşe Nazlı
relation.isOrgUnitOfPublication91bbe15d-017f-446b-b102-ce755523d939
relation.isOrgUnitOfPublicationd6cdc646-db27-4078-a933-2db6f139bb65
relation.isOrgUnitOfPublicationd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isOrgUnitOfPublication.latestForDiscovery91bbe15d-017f-446b-b102-ce755523d939
relation.isParentOrgUnitOfPublication20385dee-35e7-484b-8da6-ddcc08271d96
relation.isParentOrgUnitOfPublicationd437580f-9309-4ecb-864a-4af58309d287
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery20385dee-35e7-484b-8da6-ddcc08271d96

Files

Collections

Publications without Fulltext