Publication: The rarest subtype of a rare disease: infantile facioscapulohumeral dystrophy
dc.contributor.department | KUH (Koç University Hospital) | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Akçay, Ayfer Arduç | |
dc.contributor.kuauthor | Eraslan, Serpil | |
dc.contributor.kuauthor | Avcı, Şahin | |
dc.contributor.kuauthor | Eren, İlker | |
dc.contributor.kuauthor | Yunisova, Gulshan | |
dc.contributor.kuauthor | Özdağ, Ayşe Nur Acar | |
dc.contributor.kuauthor | Kayserili, Hülya | |
dc.contributor.kuauthor | Oflazer, Piraye | |
dc.contributor.schoolcollegeinstitute | KUH (KOÇ UNIVERSITY HOSPITAL) | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2025-03-06T20:59:46Z | |
dc.date.issued | 2024 | |
dc.description.indexedby | WOS | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.identifier.doi | 10.1016/j.nmd.2024.07.364 | |
dc.identifier.eissn | 1873-2364 | |
dc.identifier.issn | 0960-8966 | |
dc.identifier.issue | Supp 1 | |
dc.identifier.quartile | Q2 | |
dc.identifier.uri | https://doi.org/10.1016/j.nmd.2024.07.364 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/27758 | |
dc.identifier.volume | 43 | |
dc.identifier.wos | 1330908100356 | |
dc.keywords | Infantile facioscapulohumeral dystrophy (FSHD) | |
dc.keywords | Rare neuromuscular disorders | |
dc.keywords | Muscular dystrophy | |
dc.language.iso | eng | |
dc.publisher | Pergamon-Elsevier Science | |
dc.relation.ispartof | Neuromuscular Disorders | |
dc.subject | Clinical neurology | |
dc.subject | Neurosciences | |
dc.title | The rarest subtype of a rare disease: infantile facioscapulohumeral dystrophy | |
dc.type | Meeting Abstract | |
dspace.entity.type | Publication | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit1 | KUH (KOÇ UNIVERSITY HOSPITAL) | |
local.publication.orgunit2 | KUH (Koç University Hospital) | |
local.publication.orgunit2 | School of Medicine | |
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