Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia von Postma, Alex V, Denjoy, Isabelle, Hoorntje, Theo M, Lupoglazoff, Jean-Marc, Da Costa, Antoine, Sebillon, Pascale, Mannens, Marcel M.A.M, Wilde, Arthur A.M, Guicheney, Pascale

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Mutational analysis of the β- and δ-sarcoglycan genes in a large number of patients with familial and sporadic dilated cardiomyopathy von Sylvius, Nicolas, Duboscq-Bidot, Laetitia, Bouchier, Christiane, Charron, Philippe, Benaiche, Abdelaziz, Sébillon, Pascale, Komajda, Michel, Villard, Eric

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Influence of mobilized stem cells on myocardial infarct repair in a nonhuman primate model von Norol, Françoise, Merlet, Pascal, Isnard, Richard, Sebillon, Pascale, Bonnet, Nicolas, Cailliot, Christian, Carrion, Claire, Ribeiro, Maria, Charlotte, Frédéric, Pradeau, Pascal, Mayol, Jean-François, Peinnequin, André, Drouet, Michel, Safsafi, Karima, Vernant, Jean-Paul, Herodin, Francis

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COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fe... von Flavigny, Jeanne, Souchet, Michel, Sébillon, Pascale, Berrebi-Bertrand, Isabelle, Hainque, Bernard, Mallet, Alain, Bril, Antoine, Schwartz, Ketty, Carrier, Lucie

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Functional consequences of an LMNA mutation associated with a new cardiac and non‐cardiac phenotype von Charniot, Jean‐Christophe, Pascal, Cécile, Bouchier, Christiane, Sébillon, Pascale, Salama, Jeffrey, Duboscq‐Bidot, Laëtitia, Peuchmaurd, Mireille, Desnos, Michel, Artigou, Jean‐Yves, Komajda, Michel

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COOH-terminal truncated human cardiac MyBP-C alters myosin filament organization von Sébillon, Pascale, Bonne, Gisèle, Flavigny, Jeanne, Venin, Sophie, Rouche, Andrée, Fiszman, Marc, Vikstrom, Karen, Leinwand, Leslie, Carrier, Lucie, Schwartz, Ketty

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Rapid and Direct Detection of the Most Frequent Mediterranean (Beta)-Thalassemic Mutations by Multiplex Allele-Specific Enzymatic Amplification von Bienvenu, Thierry, Sebillon, Pascale

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UltraRapid Communication: Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia von Postma, Alex V, Denjoy, Isabelle, Hoorntje, Theo M, Lupoglazoff, Jean-Marc, Da Costa, Antoine, Sebillon, Pascale, Mannens, Marcel M.A.M, Wilde, Arthur A.M, Guicheney, Pascale

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Rapid and Direct Detection of the Most Frequent Mediterranean β-Thalassemic Mutations by Multiplex Allele-Specific Enzymatic Amplification von BIENVENU, THIERRY, SEBILLON, PASCALE, LABIE, DOMINIQUE, KAPLAN, JEAN CLAUDE, BELDJORD, CHERIF

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A T to G mutation in the polypyrimidine tract of the second intron of the human β-globin gene reduces in vitro splicing efficiency: evidence for an increased hnRNP C interaction von Sébillon, Pascale, Beldjord, Chérif, Kaplan, Jean-Claude, Brody, Edward, Marie, Joēlle

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