A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics

Cardiovascular Research

Volumn 57, Issue 4, 2003, Pages 1072-1078

  Groenewegen, W Antoinette ^a   Bezzina, Connie R ^b   Van Tintelen, J Peter ^a,c   Hoorntje, Theo M ^d   Mannens, Marcel M A M ^b   Wilde, Arthur A M ^b,e   Jongsma, Habo J ^a   Rook, Martin B ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^b ACADEMIC MEDICAL CENTER   (Netherlands)

^c UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^d ST ANTONIUS HOSPITAL   (Netherlands)

^e ROYAL NETHERLANDS ACADEMY OF ARTS AND SCIENCES   (Netherlands)

Author keywords

Arrhythmia (mechanisms); Biology; Long QT syndrome; Na channel

Indexed keywords

COMPLEMENTARY RNA; ISOLEUCINE; SODIUM CHANNEL; VALINE;

ARTICLE; CARBOXY TERMINAL SEQUENCE; CODON; DNA POLYMORPHISM; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC SCREENING; HUMAN; LONG QT SYNDROME; MUTATION; MUTATIONAL ANALYSIS; NONHUMAN; OOCYTE; PRIORITY JOURNAL; PROTEIN DOMAIN; VOLTAGE CLAMP; WILD TYPE; XENOPUS LAEVIS;

ADOLESCENT; ADULT; CHILD; DEATH, SUDDEN, CARDIAC; DNA MUTATIONAL ANALYSIS; ELECTROCARDIOGRAPHY; FEMALE; HUMANS; LONG QT SYNDROME; MALE; MUTATION; PEDIGREE; SODIUM CHANNELS;

EID: 0345039873     PISSN: 00086363     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0008-6363(02)00838-6     Document Type: Article

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