p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient-Reference-Cited by-同舟云学术

p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient

Published:2013-02 Issue:2 Volume:10 Page:264-272
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Núñez Lucía,Barana Adriana,Amorós Irene,de la Fuente Marta González,Dolz-Gaitón Pablo,Gómez Ricardo,Rodríguez-García Isabel,Mosquera Ignacio,Monserrat Lorenzo,Delpón Eva,Caballero Ricardo,Castro-Beiras Alfonso,Tamargo Juan

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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4. Type of SCN5A mutation determines clinical severity and degree of conduction slowing in loss-of-function sodium channelopathies;Meregalli;Heart Rhythm,2009

5. Expression and intracellular localization of an SCN5A double mutant R1232W/T1620M implicated in Brugada syndrome;Baroudi;Circ Res,2002

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