Publication:
The rarest subtype of a rare disease: infantile facioscapulohumeral dystrophy

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dc.conference.dateOCT 08-12, 2024
dc.conference.locationPrague, Czech Republic
dc.conference.organizer29th International Congress of the World-Muscle-Society (WMS)
dc.contributor.departmentKUH (Koç University Hospital)
dc.contributor.facultymemberYes
dc.contributor.kuauthorAkçay, Ayfer Arduç
dc.contributor.kuauthorEraslan, Serpil
dc.contributor.kuauthorAvcı, Şahin
dc.contributor.kuauthorEren, İlker
dc.contributor.kuauthorYunisova, Gulshan
dc.contributor.kuauthorÖzdağ, Ayşe Nur Acar
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.kuauthorOflazer, Piraye
dc.contributor.schoolcollegeinstituteKUH (KOÇ UNIVERSITY HOSPITAL)
dc.date.accessioned2025-03-06T20:59:46Z
dc.date.issued2024
dc.description.indexedbyWOS
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.identifier.WoSQuartileQ2
dc.identifier.doi10.1016/j.nmd.2024.07.364
dc.identifier.eissn1873-2364
dc.identifier.issn0960-8966
dc.identifier.urihttps://doi.org/10.1016/j.nmd.2024.07.364
dc.identifier.urihttps://hdl.handle.net/20.500.14288/27758
dc.identifier.volume43
dc.identifier.wos001330908100356
dc.keywordsInfantile facioscapulohumeral dystrophy (FSHD)
dc.keywordsRare neuromuscular disorders
dc.keywordsMuscular dystrophy
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofNeuromuscular Disorders
dc.subjectClinical neurology
dc.subjectNeurosciences
dc.titleThe rarest subtype of a rare disease: infantile facioscapulohumeral dystrophy
dc.typeMeeting Abstract
dspace.entity.typePublication
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