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

dc.contributor.coauthorTezen, Didem
dc.contributor.coauthorKhojakulov, Zakhiriddin
dc.contributor.coauthorGunduz, Aysegul
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.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.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.identifier.doi10.1007/s10072-024-07805-0
dc.identifier.eissn1590-3478
dc.identifier.issn1590-1874
dc.identifier.issue12
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85206385757
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.wos1336737800002
dc.keywordsCongenital myasthenic syndrome
dc.keywordsHereditary polyneuropathy
dc.keywordsNeuromuscular disorders
dc.keywordsCorrection
dc.language.isoeng
dc.publisherSpringer Verlag Italia
dc.relation.ispartofNeurological Sciences
dc.subjectClinical neurology
dc.subjectNeurosciences
dc.titleClinical, electrophysiological, and genetic analysis of a family with two rare neuromuscular disorders: congenital myasthenic syndrome and hereditary polyneuropathy
dc.typeOther
dc.type.otherCorrection
dspace.entity.typePublication
local.contributor.kuauthorBaşak, Ayşe Nazlı
local.publication.orgunit1SCHOOL OF MEDICINE
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local.publication.orgunit2School of Medicine
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