dc.contributor.author | Hatemi, Ali Can | |
dc.contributor.author | Ceyran, Hakan | |
dc.contributor.author | Üstek, Duran | |
dc.date.accessioned | 10.07.201910:49:13 | |
dc.date.accessioned | 2019-07-10T19:37:22Z | |
dc.date.available | 10.07.201910:49:14 | |
dc.date.available | 2019-07-10T19:37:22Z | |
dc.date.issued | 2015 | en_US |
dc.identifier.citation | Hatemi, A. C., Ceyran, H. ve Üstek, D. (2015). Determination of a new mutation in MT-ND1 gene of a patient with dextrocardia, ventriculoarterial discordance, and tricuspid atresia. Artificial Organs, 39(1), 83-84. https://dx.doi.org/10.1111/aor.12442 | en_US |
dc.identifier.issn | 0160-564X | |
dc.identifier.issn | 1525-1594 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12511/1388 | |
dc.identifier.uri | https://dx.doi.org/10.1111/aor.12442 | |
dc.description.abstract | Tricuspid atresia, a congenital heart defect (CHD) with unknown etiology, occurs 0.056 per 100 live births and is invariably associated with right ventricular hypoplasia, and atrial/ventricular septal defects (1). Recently, many of associations have been reported between mitochondrial DNA (mtDNA) and a variety of diseases (2). Next-generation sequencing has overcome many limitations of mtDNA studies, such as estimation of heteroplasmy level and its effects on the severity of mitochondrial diseases. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Blackwell Publishing | en_US |
dc.rights | info:eu-repo/semantics/embargoedAccess | en_US |
dc.subject | Congenital Heart Defect | en_US |
dc.subject | DNA | en_US |
dc.subject | mtDNA | en_US |
dc.title | Determination of a new mutation in MT-ND1 gene of a patient with dextrocardia, ventriculoarterial discordance, and tricuspid atresia | en_US |
dc.type | letter | en_US |
dc.relation.ispartof | Artificial Organs | en_US |
dc.department | İstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Tıbbi Genetik Ana Bilim Dalı | en_US |
dc.authorid | 0000-0002-0060-2859 | en_US |
dc.identifier.volume | 39 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 83 | en_US |
dc.identifier.endpage | 84 | en_US |
dc.relation.publicationcategory | Diğer | en_US |
dc.identifier.doi | 10.1111/aor.12442 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.identifier.scopusquality | Q2 | en_US |