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dc.contributor.authorFAK, ALİ SERDAR
dc.contributor.authorHancer, Veysel Sabri
dc.contributor.authorTanrikulu, Azra Meryem
dc.contributor.authorAltun, Ibrahim
dc.contributor.authorBilge, Ahmet Kaya
dc.contributor.authorDiz-Kucukkaya, Reyhan
dc.contributor.authorAdalet, Kamil
dc.contributor.authorYilmaz, Ercument
dc.contributor.authorOzben, Beste
dc.date.accessioned2021-03-03T19:03:05Z
dc.date.available2021-03-03T19:03:05Z
dc.date.issued2008
dc.identifier.citationOzben B., Altun I., Hancer V. S. , Bilge A. K. , Tanrikulu A. M. , Diz-Kucukkaya R., FAK A. S. , Yilmaz E., Adalet K., "Angiotensin-converting enzyme gene polymorphism in arrhythmogenic right ventricular dysplasia: is DD genotype helpful in predicting syncope risk?", JOURNAL OF THE RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM, cilt.9, sa.4, ss.215-220, 2008
dc.identifier.issn1470-3203
dc.identifier.otherav_5277e8eb-1150-4d05-94ee-944d2c9c18aa
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/58538
dc.identifier.urihttps://doi.org/10.1177/1470320308099126
dc.description.abstractIntroduction. Arrhythmogenic right ventricular dysplasia (ARVD) is a heritable disorder characterised by fibrofatty replacement of right ventricular myocytes and increased risk of ventricular arrhythmias and sudden cardiac death. Angiotensin-converting enzyme (ACE) gene insertion/deletion (I/D)) polymorphism affects myocardial ACE levels. DD genotype favours myocardial fibrosis and is associated with malignant ventricular tachycardia. The aim of this study was to explore ACE gene polymorphism in ARVD patients.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectSağlık Bilimleri
dc.subjectPERİFERAL VASKÜLER HASTALIĞI
dc.subjectKlinik Tıp
dc.subjectTıp
dc.titleAngiotensin-converting enzyme gene polymorphism in arrhythmogenic right ventricular dysplasia: is DD genotype helpful in predicting syncope risk?
dc.typeMakale
dc.relation.journalJOURNAL OF THE RENIN-ANGIOTENSIN-ALDOSTERONE SYSTEM
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume9
dc.identifier.issue4
dc.identifier.startpage215
dc.identifier.endpage220
dc.contributor.firstauthorID64778


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