Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).

Circulation research

Volumn 88, Issue 12, 2001, Pages

  Baroudi, G ^a   Pouliot, V ^a   Denjoy, I ^a   Guicheney, P ^a   Shrier, A ^a   Chahine, M ^a  

^a LAVAL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN SUBUNIT; SODIUM; SODIUM CHANNEL; VOLTAGE GATED NA+ CHANNEL NA(V)1.5A; VOLTAGE-GATED NA+ CHANNEL NA(V)1.5A;

AMINO ACID SUBSTITUTION; ANIMAL; ARTICLE; CELL CULTURE; CELL MEMBRANE; CHANNEL GATING; CYTOLOGY; ELECTROPHYSIOLOGY; GENE EXPRESSION; GENETIC TRANSFECTION; GENETICS; HEART BUNDLE BRANCH BLOCK; HEART VENTRICLE FIBRILLATION; HUMAN; IMMUNOHISTOCHEMISTRY; METABOLISM; MUTATION; OOCYTE; PATCH CLAMP; PATHOPHYSIOLOGY; PROTEIN TRANSPORT; SUDDEN DEATH; SYNDROME; XENOPUS;

AMINO ACID SUBSTITUTION; ANIMALS; BUNDLE-BRANCH BLOCK; CELL MEMBRANE; CELLS, CULTURED; DEATH, SUDDEN, CARDIAC; ELECTROPHYSIOLOGY; GENE EXPRESSION; HUMANS; IMMUNOHISTOCHEMISTRY; ION CHANNEL GATING; MUTATION; OOCYTES; PATCH-CLAMP TECHNIQUES; PROTEIN SUBUNITS; PROTEIN TRANSPORT; SODIUM; SODIUM CHANNELS; SYNDROME; TRANSFECTION; VENTRICULAR FIBRILLATION; XENOPUS;

EID: 0035933766     PISSN: None     EISSN: 15244571     Source Type: Journal    
DOI: None     Document Type: Article

References (0)