Publication:
Correction to: a CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry

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dc.contributor.coauthorCortese A., Beecroft S.J., Facchini S., Curro R., Cabrera-Serrano M., Stevanovski I., Chintalaphani S.R., Gamaarachchi H., Weisburd B., Folland C., Monahan G., Scriba C.K., Dofash L., Johari M., Grosz B.R., Ellis M., Fearnley L.G., Tankard R., Read J., Merve A., Dominik N., Vegezzi E., Schnekenberg R.P., Fernandez-Eulate G., Masingue M., Giovannini D., Delatycki M.B., Storey E., Gardner M., Amor D.J., Nicholson G., Vucic S., Henderson R.D., Robertson T., Dyke J., Fabian V., Mastaglia F., Davis M.R., Kennerson M., Bonne G., Chen Z., Udd B., Straub V., Carroll L., Reilly M.M., Rossor A.M., Simone R., Quartesan I., Tassorelli C., Ghia A., Manini A., Toscano A., Abati E., Corti S.P., Comi G.P., Grandis M., Danzi M.C., Zuchner S., Pellerin D., Brais B., Brady S., Pitceathly R.D.S., Wicklund M., Lilleker J.B., Malfatti E., Yeşil G., Kayserili H., Başak N.A., Oflazer P., Quinlivan R., Hammans S., Tucci A., Bahlo M., McLean C.A., Laing N.G., Stojkovic T., Houlden H., Hanna M.G., Deveson I.W., Lockhart P.J., Lamont P.J., Fahey M.C., Bugiardini E., Ravenscroft G., OPDM study group
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorOflazer, Piraye
dc.contributor.kuauthorBaşak, Ayşe Nazlı
dc.contributor.kuauthorKayserili, Hülya
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2025-03-06T20:59:34Z
dc.date.issued2024
dc.description.abstractCorrection to: Nature Communicationshttps://doi.org/10.1038/s41467-024-49950-2, published online 27 July 2024 In this article the OPDM study group member James B Lilleker was incorrectly written as James B Lilliker. The original article has been corrected.
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.identifier.doi10.1038/s41467-024-53151-2
dc.identifier.eissn2041-1723
dc.identifier.issue1
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85206680439
dc.identifier.urihttps://doi.org/10.1038/s41467-024-53151-2
dc.identifier.urihttps://hdl.handle.net/20.500.14288/27744
dc.identifier.volume15
dc.identifier.wos1309983200004
dc.keywordsCCG expansion
dc.keywordsABCD3 gene
dc.keywordsOculopharyngodistal myopathy
dc.keywordsGenetic mutation
dc.keywordsNeuromuscular disorders
dc.language.isoeng
dc.publisherNature Research
dc.relation.ispartofNature Communications
dc.subjectGenetics
dc.titleCorrection to: a CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
dc.typeOther
dc.type.otherCorrection
dspace.entity.typePublication
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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