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Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy

dc.contributor.authorFleck, E
dc.contributor.authorRegitz-Zagrosek, V
dc.contributor.authorWollnik, B
dc.contributor.authorFrantz, E
dc.contributor.authorHetzer, R
dc.contributor.authorErdmann, J
dc.contributor.authorRaible, J
dc.contributor.authorMaki-Abadi, J
dc.contributor.authorHummel, M
dc.contributor.authorHammann, J
dc.date.accessioned2021-03-03T12:08:00Z
dc.date.available2021-03-03T12:08:00Z
dc.date.issued2001
dc.identifier.citationErdmann J., Raible J., Maki-Abadi J., Hummel M., Hammann J., Wollnik B., Frantz E., Fleck E., Hetzer R., Regitz-Zagrosek V., "Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy", JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, cilt.38, sa.2, ss.322-330, 2001
dc.identifier.issn0735-1097
dc.identifier.otherav_2c1c42e3-17cc-4a7d-9b9a-5343f42dcbb0
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/34370
dc.identifier.urihttps://doi.org/10.1016/s0735-1097(01)01387-0
dc.description.abstractObjectives We studied the clinical and genetic features of hypertrophic cardiomyopathy (HCM) caused by mutations in the myosin-binding protein C gene (MYBPC3) in 110 consecutive, unrelated patients and family members of European descent.
dc.language.isoeng
dc.subjectTıp
dc.subjectKardiyoloji
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.titleSpectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy
dc.typeMakale
dc.relation.journalJOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
dc.contributor.department, ,
dc.identifier.volume38
dc.identifier.issue2
dc.identifier.startpage322
dc.identifier.endpage330
dc.contributor.firstauthorID162748


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