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dc.contributor.author박형준-
dc.date.accessioned2016-08-29T12:08:48Z-
dc.date.available2016-08-29T12:08:48Z-
dc.date.issued2016-
dc.identifier.issn1738-6586-
dc.identifier.otherOAK-16244-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/230963-
dc.description.abstract[No abstract available]-
dc.languageEnglish-
dc.publisherKorean Neurological Association-
dc.titleFirst identification of compound heterozygous FKRP mutations in a Korean patient with limb-girdle muscular dystrophy-
dc.typeLetter-
dc.relation.issue1-
dc.relation.volume12-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.indexKCI-
dc.relation.startpage121-
dc.relation.lastpage122-
dc.relation.journaltitleJournal of Clinical Neurology (Korea)-
dc.identifier.doi10.3988/jcn.2016.12.1.121-
dc.identifier.wosidWOS:000367278300018-
dc.identifier.scopusid2-s2.0-84954357448-
dc.author.googlePark H.J.-
dc.author.googleLee J.H.-
dc.author.googleShin H.Y.-
dc.author.googleKim S.M.-
dc.author.googleChoi Y.-C.-
dc.contributor.scopusid박형준(55989522800)-
dc.date.modifydate20180306081004-
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의료원 > 의료원 > Journal papers
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