Absence of a trafficking defect in R1232W/T1620M, a double SCN5A mutant responsible for Brugada syndrome

Circulation Journal

Volumn 72, Issue 6, 2008, Pages 1018-1019

  Makita, Naomasa ^a   Mochizuki, Naoki ^b   Tsutsui, Hiroyuki ^a  

^a HOKKAIDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b NATIONAL CEREBRAL AND CARDIOVASCULAR CENTER   (Japan)

Author keywords

Brugada syndrome; Na channel; Trafficking defect

Indexed keywords

MUTANT PROTEIN; SODIUM CHANNEL;

ARTICLE; BRUGADA SYNDROME; CONFOCAL MICROSCOPY; CONTROLLED STUDY; GENE; GENE MUTATION; GENETIC POLYMORPHISM; HUMAN; HUMAN CELL; MEMBRANE TRANSPORT; PATCH CLAMP; PROTEIN EXPRESSION; SCN5A GENE; SODIUM CURRENT;

BRUGADA SYNDROME; CELL MEMBRANE; HUMANS; MUSCLE PROTEINS; MUTAGENESIS, SITE-DIRECTED; PATCH-CLAMP TECHNIQUES; PLASMIDS; PROTEIN TRANSPORT; SODIUM; SODIUM CHANNELS;

EID: 45849085710     PISSN: 13469843     EISSN: 13474820     Source Type: Journal    
DOI: 10.1253/circj.72.1018     Document Type: Article

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