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dc.contributor.author박충기-
dc.date.accessioned2018-03-27T00:49:34Z-
dc.date.available2018-03-27T00:49:34Z-
dc.date.issued2013-04-
dc.identifier.citationJournal of Cardiology, 2013, 7(4), P.e119-e120en_US
dc.identifier.issn1878-5409-
dc.identifier.issn10.1016/j.jccase.2013.01.006-
dc.identifier.urihttp://www.sciencedirect.com/science/article/pii/S1878540913000200?via%3Dihub-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/52824-
dc.description.abstractWe read with interest the report by Lee et al. entitled “Congenital anomaly of the true double-lumen right coronary artery: an extremely rare case” [1]. Previously reported cases of the double right coronary artery (DRCA) mostly described anomalies with a common proximal right coronary artery (RCA) that diverged into two separate distal branches. Meanwhile, the current case described by Lee et al. is a type of fenestrated RCA anomaly in which the common proximal RCA diverges into two separated branches proximally and converges back to a common lumen distally.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.titleCongenital anomaly of the true double-lumen right coronary artery: An extremely rare caseen_US
dc.typeArticleen_US
dc.relation.no4-
dc.relation.volume7-
dc.relation.page119-120-
dc.relation.journalJournal of Cardiology Cases-
dc.contributor.googleauthorPark, Choong-Ki-
dc.contributor.googleauthorKim, Jinoo-
dc.contributor.googleauthorKim, Ji Eun-
dc.relation.code2013038673-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidckpark1-
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COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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