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Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.
Published in:
2016
By:
- Portero, Vincent;
- Le Scouarnec, Solena;
- Es ‐ Salah ‐ Lamoureux, Zeineb;
- Burel, Sophie;
- Gourraud, Jean ‐ Baptiste;
- Bonnaud, Stéphanie;
- Lindenbaum, Pierre;
- Simonet, Floriane;
- Violleau, Jade;
- Baron, Estelle;
- Moreau, Eléonore;
- Scott, Carol;
- Chatel, Stéphanie;
- Loussouarn, Gildas;
- O'Hara, Thomas;
- Mabo, Philippe;
- Dina, Christian;
- Le Marec, Hervé;
- Schott, Jean ‐ Jacques;
- Probst, Vincent
Publication type:
journal article
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.
Published in:
Human Molecular Genetics, 2015, v. 24, n. 10, p. 2757, doi. 10.1093/hmg/ddv036
By:
- Le Scouarnec, Solena;
- Karakachoff, Matilde;
- Gourraud, Jean-Baptiste;
- Lindenbaum, Pierre;
- Bonnaud, Stéphanie;
- Portero, Vincent;
- Duboscq-Bidot, Laëtitia;
- Daumy, Xavier;
- Simonet, Floriane;
- Teusan, Raluca;
- Baron, Estelle;
- Violleau, Jade;
- Persyn, Elodie;
- Bellanger, Lise;
- Barc, Julien;
- Chatel, Stéphanie;
- Martins, Raphaël;
- Mabo, Philippe;
- Sacher, Frédéric;
- Haïssaguerre, Michel
Publication type:
Article
Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form‐associated genes provides new insights for molecular diagnosis and clinical management.
Published in:
Human Mutation, 2022, v. 43, n. 9, p. 1333, doi. 10.1002/humu.24436
By:
- Goudal, Adeline;
- Karakachoff, Matilde;
- Lindenbaum, Pierre;
- Baron, Estelle;
- Bonnaud, Stéphanie;
- Kyndt, Florence;
- Arnaud, Marine;
- Minois, Damien;
- Bourcereau, Emmanuelle;
- Thollet, Aurélie;
- Deleuze, Jean‐François;
- Genin, Emmanuelle;
- Wiart, François;
- Pasquié, Jean‐Luc;
- Galand, Vincent;
- Sacher, Frédéric;
- Dina, Christian;
- Redon, Richard;
- Bezieau, Stéphane;
- Schott, Jean‐Jacques
Publication type:
Article

Found: 3

Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.

Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.

Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form‐associated genes provides new insights for molecular diagnosis and clinical management.