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dc.contributor.authorJ Gordon Millichap
dc.contributor.otherNorthwestern University Feinberg School of Medicine
dc.date.accessioned2015-11-23T03:00:05Z
dc.date.available2025-10-02T04:42:14Z
dc.date.issued01-01-2009
dc.identifier.issn-
dc.identifier.urihttps://www.pediatricneurologybriefs.com/articles/233
dc.description.abstractThe CHRNE e1293insG mutation was identified in 14 (60%) of 23 North African families with an early onset form of congenital myasthenic syndrome studied at centers in France, Tunisia, Algeria, and UK.
dc.format-
dc.language.isoEN
dc.publisherPediatric Neurology Briefs Publishers
dc.relation.uri['https://ejo.springeropen.com/', 'https://ejo.springeropen.com/submission-guidelines', 'https://ejo.springeropen.com/about']
dc.rightsCC BY
dc.subject['rhinology', 'head and neck', 'otology', 'audiology', 'otorhinolaryngology', 'phoniatrics', 'Otorhinolaryngology', 'RF1-547']
dc.subject.lccPediatrics
dc.titleCHRNE Mutation and Congenital Myasthenia
dc.typeArticle
dc.description.keywordsoculobulbar involvement
dc.description.keywordsmild and stable course
dc.description.keywordscholinesterase inhibitors
dc.description.pages7-7
dc.description.doi10.15844/pedneurbriefs-23-1-8
dc.title.journalPediatric Neurology Briefs
dc.identifier.e-issn2166-6482
dc.identifier.oaioai:doaj.org/journal:4e8a9e579d354c7d9f32f5d1c336b9c6
dc.journal.infoVolume 23, Issue 1


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