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Autor:
Rivaud, M.R. (Mathilde R.), Marchal, G.A. (Gerard A.), Wolswinkel, R. (Rianne), Jansen, J.A. (John A.), van-der-Made, I. (Ingeborg), Beekman, L. (Leander), Ruiz-Villalba, A. (Adrián), Baartscheer, A. (Antonius), Rajamani, S. (Sridharan), Belardinelli, L. (Luiz), van-Veen, T.A.B. (Toon A.B.), Basso, C. (Cristina), Thiene, G. (Gaetano), Creemers, E.E. (Ester E.), Bezzina, C.R. (Connie R.), Remme, C.A. (Carol Ann)
Aims SCN5A mutations are associated with arrhythmia syndromes, including Brugada syndrome, long QT syndrome type 3 (LQT3), and cardiac conduction disease. Long QT syndrome type 3 patients display atrio-ventricular (AV) conduction slowing which may co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1111::eab02bcee033fac3bdd11a609332a2d9
https://hdl.handle.net/10171/66321
https://hdl.handle.net/10171/66321