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Delinière, Antoine; Haddad, Christelle; Herrera-Siklody, Claudia; Hermida, Alexis; Pruvot, Etienne; Bressieux-Degueldre, Sabrina; Millat, Gilles; Janin, Alexandre; Hermida, Jean-Sylvain; Asatryan, Babken; Chevalier, Philippe (2023). Phenotypic Characterization of Timothy Syndrome Caused by the CACNA1C p.Gly402Ser Variant. Circulation. Genomic and precision medicine, 16(3), pp. 280-282. American Heart Association 10.1161/CIRCGEN.122.004010
Chevalier, Philippe; Moreau, Adrien; Bessière, Francis; Richard, Sylvain; Chahine, Mohamed; Millat, Gilles; Morel, Elodie; Paganelli, Franck; Lesavre, Nathalie; Placide, Leslie; Montestruc, François; Ankou, Bénédicte; Puertas, Rosa Doñate; Asatryan, Babken; Delinière, Antoine (2023). Identification of Cx43 variants predisposing to ventricular fibrillation in the acute phase of ST-elevation myocardial infarction. Europace, 25(1), pp. 101-111. Oxford University Press 10.1093/europace/euac128
Liu, Hui; Chatel, Stéphanie; Simard, Christophe; Syam, Ninda; Salle, Laurent; Probst, Vincent; Morel, Julie; Millat, Gilles; Lopez, Michel; Abriel, Hugues; Schott, Jean-Jacques; Guinamard, Romain; Bouvagnet, Patrice (2013). Molecular genetics and functional anomalies in a series of 248 Brugada cases with 11 mutations in the TRPM4 channel. PLoS ONE, 8(1), e54131. Public Library of Science 10.1371/journal.pone.0054131
