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dc.contributor.authorKyriakogonas, Stavros
dc.contributor.authorStefanadis, Christodoulos
dc.contributor.authorKotta, Christina-Maria
dc.contributor.authorWollnik, Bernd
dc.contributor.authorTheopistou, Artemisia
dc.contributor.authorAnastasakis, Aris
dc.date.accessioned2021-03-03T19:04:54Z
dc.date.available2021-03-03T19:04:54Z
dc.date.issued2006
dc.identifier.citationAnastasakis A., Kotta C., Kyriakogonas S., Wollnik B., Theopistou A., Stefanadis C., "Phenotype reveals genotype in a Greek long QT syndrome family", EUROPACE, cilt.8, sa.4, ss.241-244, 2006
dc.identifier.issn1099-5129
dc.identifier.otherav_52a32131-a131-4d66-9b13-1fa30021d151
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/58651
dc.identifier.urihttps://doi.org/10.1093/europace/eul012
dc.description.abstractWe aimed to verify the tong QT syndrome (LQTS) genotype in a family with strong evidence of LQTS type 1 (LQT1) on the basis of so far established genotype-phenotype correlations. Genetic testing for mutations in the KCNQ1 potassium channel gene revealed an A341V mutation in three generations of the family. Existing genotype-phenotype correlations were correctly predictive of the genotype in the case of this family, despite the fact that there are no previously reported data for the Greek LQTS genetic pool. Thus, genotype-phenotype correlations are often a helpful tool in the management of LQTS patients and their families.
dc.language.isoeng
dc.subjectKardiyoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.titlePhenotype reveals genotype in a Greek long QT syndrome family
dc.typeMakale
dc.relation.journalEUROPACE
dc.contributor.department, ,
dc.identifier.volume8
dc.identifier.issue4
dc.identifier.startpage241
dc.identifier.endpage244
dc.contributor.firstauthorID178382


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