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dc.contributor.author구혜수-
dc.date.accessioned2016-08-28T11:08:21Z-
dc.date.available2016-08-28T11:08:21Z-
dc.date.issued2015-
dc.identifier.issn1738-6586-
dc.identifier.otherOAK-12334-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/228509-
dc.description.abstractCharcot-Marie-Tooth disease; Dejerine-Sottas neuropathy; Periaxin; Peripheral nerve; Whole-exome sequencing-
dc.languageEnglish-
dc.publisherKorean Neurological Association-
dc.titleNovel compound heterozygous nonsense prx mutations in a korean dejerine-sottas neuropathy family-
dc.typeArticle-
dc.relation.issue1-
dc.relation.volume11-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.indexKCI-
dc.relation.startpage92-
dc.relation.lastpage96-
dc.relation.journaltitleJournal of Clinical Neurology (Korea)-
dc.identifier.doi10.3988/jcn.2015.11.1.92-
dc.identifier.wosidWOS:000347511500013-
dc.identifier.scopusid2-s2.0-84923377639-
dc.author.googleChoi Y.J.-
dc.author.googleHyun Y.S.-
dc.author.googleNam S.H.-
dc.author.googleKoo H.-
dc.author.googleHong Y.B.-
dc.author.googleChung K.W.-
dc.author.googleChoi B.-O.-
dc.contributor.scopusid구혜수(7102121023;57217717081;56612832400)-
dc.date.modifydate20221202111401-
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의과대학 > 의학과 > Journal papers
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