Please use this identifier to cite or link to this item: https://hdl.handle.net/1/2388
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dc.contributor.authorEl-Wahsh, Shadi-
dc.contributor.authorWijesinghe, Rajiv-
dc.contributor.authorQiu, Jessica-
dc.contributor.authorHeard, Robert-
dc.contributor.authorStoll, Marion-
dc.contributor.authorReddel, Stephen-
dc.date.accessioned2023-08-31T02:36:28Z-
dc.date.available2023-08-31T02:36:28Z-
dc.date.issued2023-09-
dc.identifier.citation68(3):E32-E34en
dc.identifier.urihttps://hdl.handle.net/1/2388-
dc.description.abstractNo abstract available.en
dc.description.sponsorshipNeurologyen
dc.subjectNeurologyen
dc.subjectBrainen
dc.titleVery late-onset limb-girdle congenital myasthenic syndrome due to GFPT1 mutationen
dc.typeJournal Articleen
dc.identifier.doi10.1002/mus.27842en
dc.description.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/37403580en
dc.description.affiliatesGosford Hospitalen
dc.identifier.journaltitleMuscle & Nerveen
dc.type.studyortrialCase Series and Case Reportsen
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
crisitem.author.deptNeurology-
Appears in Collections:Neurology
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