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Ausgangspunkt war und ist immer noch der Patient mit seiner Familie, z.\u202fB. mit einer famili\u00e4ren Arrhythmieform oder einer Kardiomyopathie, die Aufkl\u00e4rung der genetischen Ursache und die personalisierte Behandlung der Betroffenen.\u00a0\u00a0Das wissenschaftliche, immer transnational orientierte Interesse, ein urs\u00e4chliches Gen zu identifizieren und den zugrundeliegenden Pathomechanismus aufzudecken, hat beim Brugada-Syndrom, Kurzen QT-Syndrom und Erregungsleitungsst\u00f6rung oder Sinusknotendysfunktion, aber auch bei DCM oder ARVC zu beachteten Beitr\u00e4gen gef\u00fchrt. Wichtig ist jedoch der Weg zur\u00fcck (bench &gt; bed side): Implementierung von nationalen wie internationalen Empfehlungen zur kardiogenetischen Diagnostik in die kardiologische Versorgung und die personalisierte Betreuung und Therapie Betroffener.<\/jats:p>","DOI":"10.1007\/s00399-024-01008-y","type":"journal-article","created":{"date-parts":[[2024,2,28]],"date-time":"2024-02-28T18:02:32Z","timestamp":1709143352000},"page":"127-137","update-policy":"http:\/\/dx.doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Kardiogenetik in Deutschland\u00a0\u2013 ein (R\u00fcck\u2011)Blick","Cardiogenetics in Germany\u2014 a view and review"],"prefix":"10.1007","volume":"35","author":[{"given":"E.","family":"Schulze-Bahr","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2024,2,28]]},"reference":[{"key":"1008_CR1","first-page":"291","volume":"14","author":"Anonymous","year":"1973","unstructured":"Anonymous (1973) The jervell and Lange-Nielsen syndrome and its variations. 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