TAD boundary deletion causes PITX2-related cardiac electrical and structural defects von Baudic, Manon, Murata, Hiroshige, Bosada, Fernanda M., Melo, Uirá Souto, Aizawa, Takanori, Lindenbaum, Pierre, van der Maarel, Lieve E., Guedon, Amaury, Baron, Estelle, Fremy, Enora, Foucal, Adrien, Ishikawa, Taisuke, Ushinohama, Hiroya, Jurgens, Sean J., Choi, Seung Hoan, Kyndt, Florence, Le Scouarnec, Solena, Wakker, Vincent, Thollet, Aurélie, Rajalu, Annabelle, Takaki, Tadashi, Ohno, Seiko, Shimizu, Wataru, Horie, Minoru, Kimura, Takeshi, Ellinor, Patrick T., Petit, Florence, Dulac, Yves, Bru, Paul, Boland, Anne, Deleuze, Jean-François, Redon, Richard, Le Marec, Hervé, Le Tourneau, Thierry, Gourraud, Jean-Baptiste, Yoshida, Yoshinori, Makita, Naomasa, Vieyres, Claude, Makiyama, Takeru, Mundlos, Stephan, Christoffels, Vincent M., Probst, Vincent, Schott, Jean-Jacques, Barc, Julien

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Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease von Le Scouarnec, Solena, Bhasin, Naina, Vieyres, Claude, Hund, Thomas J, Cunha, Shane R, Koval, Olha, Marionneau, Celine, Chen, Biyi, Wu, Yuejin, Demolombe, Sophie, Song, Long-Sheng, Le Marec, Hervé, Probst, Vincent, Schott, Jean-Jacques, Anderson, Mark E, Mohler, Peter J

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Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome von Barc, Julien, PhD, Briec, François, MD, Schmitt, Sébastien, MD, Kyndt, Florence, PharmD, PhD, Le Cunff, Martine, BS, Baron, Estelle, BS, Vieyres, Claude, MD, Sacher, Frédéric, MD, Redon, Richard, PhD, Le Caignec, Cédric, MD, PhD, Le Marec, Hervé, MD, PhD, Probst, Vincent, MD, PhD, Schott, Jean-Jacques, PhD

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BS-515-01 NON-CODING DELETION INDUCES 3D CHROMATIN REMODELLING AND PITX2 EXPRESSION DYSREGULATION ASSOCIATED WITH A SYNDROMIC CARDIAC DISORDER von Baudic, Manon, Murata, Hiroshige, Bosada, Fernanda M., Melo, Uira Souto, Ishikawa, Taisuke, Aizawa, Takanori, Guedon, Amaury, Baron, Estelle, FOUCAL, ADRIEN, Lindenbaum, Pierre, Le Scouarnec, Solena, Shimizu, Wataru, GOURRAUD, JEAN BAPTISTE, Makita, Naomasa, Le Marec, Herve, Vieyres, Claude, Mundlos, Stephan, Christoffels, Vincent M., Makiyama, Takeru, PROBST, VINCENT, Schott, Jean-Jacques, Barc, Julien

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Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance von Barc, Julien, Briec, François, Schmitt, Sébastien, Kyndt, Florence, Le Cunff, Martine, Baron, Estelle, Vieyres, Claude, Sacher, Frédéric, Redon, Richard, Le Caignec, Cédric, Le Marec, Hervé, Probst, Vincent, Schott, Jean-Jacques

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Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a new syndromic cardiac disorder von Baudic, Manon, Murata, Hiroshigue, Bosada, Fernanda, Melo, Uirá Souto, Ishikawa, Taisuke, Aizawa, Takanori, Guedon, Amaury, Baron, Estelle, Foucal, Adrien, Lindenbaum, Pierre, Le Scouarnec, Solena, Makita, Naomasa, Le Marec, Hervé, Vieyres, Claude, Mundlos, Stephan, Christoffels, Vincent M., Makiyama, Takeru, Probst, Vincent, Schott, Jean-Jacques, Barc, Julien

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Screening for Copy Number Variation in Genes Associated With the Long QT Syndrome: Clinical Relevance von BARC, Julien, BRIEC, François, LE MAREC, Herve, PROBST, Vincent, SCHOTT, Jean-Jacques, SCHMITT, Sébastien, KYNDT, Florence, LE CUNFF, Martine, BARON, Estelle, VIEYRES, Claude, SACHER, Frederic, REDON, Richard, LE CAIGNEC, Cedric

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