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	1.	Non-syndromic Mitral Valve Dysplasia Mutation Changes the Force Resilience and Interaction of Human Filamin A. [electronic resource] by Haataja, Tatu J K Bernardi, Rafael C Lecointe, Simon Capoulade, Romain Merot, Jean Pentikäinen, Ulla Producer: 20200221 In: Structure (London, England : 1993) vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Critical Structural Defects Explain Filamin A Mutations Causing Mitral Valve Dysplasia. [electronic resource] by Haataja, Tatu J K Capoulade, Romain Lecointe, Simon Hellman, Maarit Merot, Jean Permi, Perttu Pentikäinen, Ulla Producer: 20200929 In: Biophysical journal vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Filamin-a-related myxomatous mitral valve dystrophy: genetic, echocardiographic and functional aspects. [electronic resource] by Lardeux, Aurélie Kyndt, Florence Lecointe, Simon Marec, Hervé Le Merot, Jean Schott, Jean-Jacques Le Tourneau, Thierry Probst, Vincent Producer: 20120312 In: Journal of cardiovascular translational research vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The alternatively spliced LRRFIP1 Isoform-1 is a key regulator of the Wnt/β-catenin transcription pathway. [electronic resource] by Labbé, Pauline Faure, Emilie Lecointe, Simon Le Scouarnec, Solena Kyndt, Florence Marrec, Marie Le Tourneau, Thierry Offmann, Bernard Duplaà, Cécile Zaffran, Stéphane Schott, Jean Jacques Merot, Jean Producer: 20171024 In: Biochimica et biophysica acta. Molecular cell research vol. 1864 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Identification of novel APOB mutations by targeted next-generation sequencing for the molecular diagnosis of familial hypobetalipoproteinemia. [electronic resource] by Rimbert, Antoine Pichelin, Matthieu Lecointe, Simon Marrec, Marie Le Scouarnec, Solena Barrak, Elias Croyal, Mikael Krempf, Michel Le Marec, Hervé Redon, Richard Schott, Jean-Jacques Magré, Jocelyne Cariou, Bertrand Producer: 20171220 In: Atherosclerosis vol. 250 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations. [electronic resource] by Béziau, Delphine M Barc, Julien O'Hara, Thomas Le Gloan, Laurianne Amarouch, Mohamed Yassine Solnon, Aude Pavin, Dominique Lecointe, Simon Bouillet, Patricia Gourraud, Jean-Baptiste Guicheney, Pascale Denjoy, Isabelle Redon, Richard Mabo, Philippe le Marec, Hervé Loussouarn, Gildas Kyndt, Florence Schott, Jean-Jacques Probst, Vincent Baró, Isabelle Producer: 20150526 In: Basic research in cardiology vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Fine-scale human genetic structure in Western France. [electronic resource] by Karakachoff, Matilde Duforet-Frebourg, Nicolas Simonet, Floriane Le Scouarnec, Solena Pellen, Nadine Lecointe, Simon Charpentier, Eric Gros, Françoise Cauchi, Stéphane Froguel, Philippe Copin, Nane Le Tourneau, Thierry Probst, Vincent Le Marec, Hervé Molinaro, Sabrina Balkau, Beverley Redon, Richard Schott, Jean-Jacques Blum, Michael Gb Dina, Christian Producer: 20160203 In: European journal of human genetics : EJHG vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Genetic Association Analyses Highlight [electronic resource] by Thériault, Sébastien Dina, Christian Messika-Zeitoun, David Le Scouarnec, Solena Capoulade, Romain Gaudreault, Nathalie Rigade, Sidwell Li, Zhonglin Simonet, Floriane Lamontagne, Maxime Clavel, Marie-Annick Arsenault, Benoit J Boureau, Anne-Sophie Lecointe, Simon Baron, Estelle Bonnaud, Stéphanie Karakachoff, Matilde Charpentier, Eric Fellah, Imen Roussel, Jean-Christian Philippe Verhoye, Jean Baufreton, Christophe Probst, Vincent Roussel, Ronan Redon, Richard Dagenais, François Pibarot, Philippe Mathieu, Patrick Le Tourneau, Thierry Bossé, Yohan Schott, Jean-Jacques Producer: 20200827 In: Circulation. Genomic and precision medicine vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome study. [electronic resource] by Le Tourneau, Thierry Le Scouarnec, Solena Cueff, Caroline Bernstein, Daniel Aalberts, Jan J J Lecointe, Simon Mérot, Jean Bernstein, Jonathan A Oomen, Toon Dina, Christian Karakachoff, Matilde Desal, Hubert Al Habash, Ousama Delling, Francesca N Capoulade, Romain Suurmeijer, Albert J H Milan, David Norris, Russell A Markwald, Roger Aikawa, Elena Slaugenhaupt, Susan A Jeunemaitre, Xavier Hagège, Albert Roussel, Jean-Christian Trochu, Jean-Noël Levine, Robert A Kyndt, Florence Probst, Vincent Le Marec, Hervé Schott, Jean-Jacques Producer: 20191118 In: European heart journal vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Genetic association analyses highlight biological pathways underlying mitral valve prolapse. [electronic resource] by Dina, Christian Bouatia-Naji, Nabila Tucker, Nathan Delling, Francesca N Toomer, Katelynn Durst, Ronen Perrocheau, Maelle Fernandez-Friera, Leticia Solis, Jorge Le Tourneau, Thierry Chen, Ming-Huei Probst, Vincent Bosse, Yohan Pibarot, Philippe Zelenika, Diana Lathrop, Mark Hercberg, Serge Roussel, Ronan Benjamin, Emelia J Bonnet, Fabrice Lo, Su Hao Dolmatova, Elena Simonet, Floriane Lecointe, Simon Kyndt, Florence Redon, Richard Le Marec, Hervé Froguel, Philippe Ellinor, Patrick T Vasan, Ramachandran S Bruneval, Patrick Markwald, Roger R Norris, Russell A Milan, David J Slaugenhaupt, Susan A Levine, Robert A Schott, Jean-Jacques Hagege, Albert A Jeunemaitre, Xavier Producer: 20151230 In: Nature genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. [electronic resource] by Bezzina, Connie R Barc, Julien Mizusawa, Yuka Remme, Carol Ann Gourraud, Jean-Baptiste Simonet, Floriane Verkerk, Arie O Schwartz, Peter J Crotti, Lia Dagradi, Federica Guicheney, Pascale Fressart, Véronique Leenhardt, Antoine Antzelevitch, Charles Bartkowiak, Susan Borggrefe, Martin Schimpf, Rainer Schulze-Bahr, Eric Zumhagen, Sven Behr, Elijah R Bastiaenen, Rachel Tfelt-Hansen, Jacob Olesen, Morten Salling Kääb, Stefan Beckmann, Britt M Weeke, Peter Watanabe, Hiroshi Endo, Naoto Minamino, Tohru Horie, Minoru Ohno, Seiko Hasegawa, Kanae Makita, Naomasa Nogami, Akihiko Shimizu, Wataru Aiba, Takeshi Froguel, Philippe Balkau, Beverley Lantieri, Olivier Torchio, Margherita Wiese, Cornelia Weber, David Wolswinkel, Rianne Coronel, Ruben Boukens, Bas J Bézieau, Stéphane Charpentier, Eric Chatel, Stéphanie Despres, Aurore Gros, Françoise Kyndt, Florence Lecointe, Simon Lindenbaum, Pierre Portero, Vincent Violleau, Jade Gessler, Manfred Tan, Hanno L Roden, Dan M Christoffels, Vincent M Le Marec, Hervé Wilde, Arthur A Probst, Vincent Schott, Jean-Jacques Dina, Christian Redon, Richard Producer: 20131126 In: Nature genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)