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Long-QT syndrome: A genetically heterogeneous ion channel disease

dc.contributor.authorWollnik, B
dc.date.accessioned2021-03-05T10:43:10Z
dc.date.available2021-03-05T10:43:10Z
dc.identifier.citationWollnik B., "Long-QT syndrome: A genetically heterogeneous ion channel disease", Conference on New Informations from Molecular Biology Methods, Munich, Almanya, 25 - 26 Ekim 1996, ss.251-259
dc.identifier.othervv_1032021
dc.identifier.otherav_a498b5ef-04c1-4b82-8ecb-afd4cf5da4e6
dc.identifier.urihttp://hdl.handle.net/20.500.12627/110099
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectKardiyoloji
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectTemel Bilimler
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.subjectKlinik Tıp
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.titleLong-QT syndrome: A genetically heterogeneous ion channel disease
dc.typeBildiri
dc.contributor.department, ,
dc.contributor.firstauthorID122061


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