Screening for mutations in human cardiomyopathy- is RBM24 a new but rare disease gene? by Anna Gaertner, Andreas Brodehl, Hendrik Milting

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RBM20 mutations in left ventricular non‐compaction cardiomyopathy by Anna Gaertner, Bärbel Klauke, Andreas Brodehl, Hendrik Milting

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In vitro functional analyses of arrhythmogenic right ventricular cardiomyopathy-associated desmoglein-2-missense variations. by Anna Gaertner, Baerbel Klauke, Ines Stork, Karsten Niehaus, Gesa Niemann, Jan Gummert, Hendrik Milting

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Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processing by Greta Marie Pohl, Manuel Göz, Anna Gaertner, Andreas Brodehl, Tolga Cimen, Ardan M. Saguner, Eric Schulze-Bahr, Volker Walhorn, Dario Anselmetti, Hendrik Milting

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Compound Heterozygous <i>FKTN</i> Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern by Anna Gaertner, Lidia Burr, Baerbel Klauke, Andreas Brodehl, Kai Thorsten Laser, Karin Klingel, Jens Tiesmeier, Uwe Schulz, Edzard zu Knyphausen, Jan Gummert, Hendrik Milting

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The Desmin Mutation <i>DES</i>-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3 by Andreas Brodehl, Carsten Hain, Franziska Flottmann, Sandra Ratnavadivel, Anna Gaertner, Bärbel Klauke, Jörn Kalinowski, Hermann Körperich, Jan Gummert, Lech Paluszkiewicz, Marcus-André Deutsch, Hendrik Milting

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The Combined Human Genotype of Truncating <i>TTN</i> and <i>RBM20</i> Mutations Is Associated with Severe and Early Onset of Dilated Cardiomyopathy by Anna Gaertner, Julia Bloebaum, Andreas Brodehl, Baerbel Klauke, Katharina Sielemann, Astrid Kassner, Henrik Fox, Michiel Morshuis, Jens Tiesmeier, Uwe Schulz, Ralph Knoell, Jan Gummert, Hendrik Milting

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Generation of a TMEM43 knockout human induced pluripotent stem cell line (HDZi003-A-1) using CRISPR/Cas9 by Sandra Ratnavadivel, Joline Dammeier, Anna Gaertner, Marcelo A. Szymanski de Toledo, Martin Zenke, Jan Gummert, Torsten Bloch Rasmussen, Nora Klinke, Kai Jürgens, Heiko Meyer, Achim Paululat, Hendrik Milting

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Molecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy by Anna Gaertner‐Rommel, Jens Tiesmeier, Thomas Jakob, Bernd Strickmann, Gunter Veit, Bernd Bachmann‐Mennenga, Lech Paluszkiewicz, Karin Klingel, Uwe Schulz, Kai T. Laser, Bernd Karger, Heidi Pfeiffer, Hendrik Milting

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High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation. by Baerbel Klauke, Anna Gaertner-Rommel, Uwe Schulz, Astrid Kassner, Edzard Zu Knyphausen, Thorsten Laser, Deniz Kececioglu, Lech Paluszkiewicz, Ute Blanz, Eugen Sandica, Antoon J van den Bogaerdt, J Peter van Tintelen, Jan Gummert, Hendrik Milting

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