A novel SCN5A mutation demonstrating a variety of clinical phenotypes in familial sick sinus syndrome

Internal Medicine

Volumn 52, Issue 16, 2013, Pages 1805-1808

  Nakajima, Seiko ^a   Makiyama, Takeru ^b   Hanazawa, Koji ^a   Kaitani, Kazuaki ^a   Amano, Masashi ^a   Hayama, Yukiko ^a   Onishi, Naoaki ^a   Tamaki, Yodo ^a   Miyake, Makoto ^a   Tamura, Toshihiro ^a   Kondo, Hirokazu ^a   Motooka, Makoto ^a   Izumi, Chisato ^a   Nakagawa, Yoshihisa ^a   Horie, Minoru ^c  

^a TENRI HOSPITAL   (Japan)

^b KYOTO UNIVERSITY   (Japan)

^c SHIGA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

Author keywords

Brugada syndrome; Overlap syndrome; SCN5A; Sick sinus syndrome

Indexed keywords

PILSICAINIDE;

ADOLESCENT; ARTICLE; BRUGADA SYNDROME; CASE REPORT; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; DNA SEQUENCE; GENE; GENE MUTATION; HEART ELECTROPHYSIOLOGY; HEART VENTRICLE TACHYCARDIA; HUMAN; IMPLANTABLE CARDIOVERTER DEFIBRILLATOR; IMPLANTED HEART PACEMAKER; MALE; MUTATIONAL ANALYSIS; PHENOTYPE; QRS COMPLEX; SCN5A GENE; SICK SINUS SYNDROME; ST SEGMENT ELEVATION;

ADOLESCENT; FEMALE; HUMANS; MALE; MUTATION; NAV1.5 VOLTAGE-GATED SODIUM CHANNEL; PEDIGREE; PHENOTYPE; SICK SINUS SYNDROME; YOUNG ADULT;

EID: 84881573874     PISSN: 09182918     EISSN: 13497235     Source Type: Journal    
DOI: 10.2169/internalmedicine.52.0085     Document Type: Article

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