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Mutational spectrum in eight Korean patients with 3-methylcrotonyl-CoA carboxylase deficiency

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dc.contributor.authorCho, S. Y.-
dc.contributor.authorPark, H-D-
dc.contributor.authorLee, Y-W-
dc.contributor.authorKi, C-S-
dc.contributor.authorLee, S-Y-
dc.contributor.authorSohn, Y. B.-
dc.contributor.authorPark, S. W.-
dc.contributor.authorKim, S. H.-
dc.contributor.authorJi, S.-
dc.contributor.authorKim, S. J.-
dc.contributor.authorChoi, E. W.-
dc.contributor.authorKim, C. H.-
dc.contributor.authorKo, A-r-
dc.contributor.authorPaik, K-H-
dc.contributor.authorLee, D. H.-
dc.contributor.authorJin, D-K-
dc.date.accessioned2021-08-12T03:46:05Z-
dc.date.available2021-08-12T03:46:05Z-
dc.date.issued2012-01-
dc.identifier.issn0009-9163-
dc.identifier.issn1399-0004-
dc.identifier.urihttps://scholarworks.bwise.kr/sch/handle/2021.sw.sch/15467-
dc.format.extent3-
dc.language영어-
dc.language.isoENG-
dc.publisherBlackwell Publishing Inc.-
dc.titleMutational spectrum in eight Korean patients with 3-methylcrotonyl-CoA carboxylase deficiency-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1111/j.1399-0004.2011.01704.x-
dc.identifier.scopusid2-s2.0-83355177176-
dc.identifier.wosid000297925600015-
dc.identifier.bibliographicCitationClinical Genetics, v.81, no.1, pp 96 - 98-
dc.citation.titleClinical Genetics-
dc.citation.volume81-
dc.citation.number1-
dc.citation.startPage96-
dc.citation.endPage98-
dc.type.docTypeLetter-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.subject.keywordPlusMCCA-
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College of Medicine > Department of Pediatrics > 1. Journal Articles
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