Cited 4 times in
Two novel frame shift mutations in lecithin:cholesterol acyltransferase (LCAT) gene associated with a familial LCAT deficiency phenotype
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 안영수 | - |
dc.date.accessioned | 2015-04-24T16:55:55Z | - |
dc.date.available | 2015-04-24T16:55:55Z | - |
dc.date.issued | 2009 | - |
dc.identifier.issn | 0021-9150 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/104441 | - |
dc.description.statementOfResponsibility | open | - |
dc.format.extent | 346~348 | - |
dc.relation.isPartOf | ATHEROSCLEROSIS | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Corneal Opacity/genetics | - |
dc.subject.MESH | Frameshift Mutation | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Lecithin Cholesterol Acyltransferase Deficiency/genetics* | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Phosphatidylcholine-Sterol O-Acyltransferase/genetics* | - |
dc.title | Two novel frame shift mutations in lecithin:cholesterol acyltransferase (LCAT) gene associated with a familial LCAT deficiency phenotype | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Pharmacology (약리학) | - |
dc.contributor.googleauthor | Cheol Whee Park | - |
dc.contributor.googleauthor | Mi-Hyun Lim | - |
dc.contributor.googleauthor | Dong-Ye Youn | - |
dc.contributor.googleauthor | Seung Eun Jung | - |
dc.contributor.googleauthor | Sungjin Chung | - |
dc.contributor.googleauthor | Young Soo Ahn | - |
dc.contributor.googleauthor | Yoon Sik Chang | - |
dc.contributor.googleauthor | Jeong-Hwa Lee | - |
dc.identifier.doi | 10.1016/j.atherosclerosis.2009.03.001 | - |
dc.admin.author | false | - |
dc.admin.mapping | false | - |
dc.contributor.localId | A02246 | - |
dc.relation.journalcode | J00260 | - |
dc.identifier.eissn | 1879-1484 | - |
dc.identifier.pmid | 19329119 | - |
dc.identifier.url | http://www.sciencedirect.com/science/article/pii/S0021915009001543 | - |
dc.subject.keyword | Familial LCAT deficiency | - |
dc.subject.keyword | LCAT gene mutation | - |
dc.subject.keyword | Compound heterozygous mutation | - |
dc.subject.keyword | High-density lipoprotein | - |
dc.contributor.alternativeName | Ahn, Young Soo | - |
dc.contributor.affiliatedAuthor | Ahn, Young Soo | - |
dc.citation.volume | 206 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 346 | - |
dc.citation.endPage | 348 | - |
dc.identifier.bibliographicCitation | ATHEROSCLEROSIS, Vol.206(2) : 346-348, 2009 | - |
dc.identifier.rimsid | 54118 | - |
dc.type.rims | ART | - |
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