From mutation to clinical presentation: Mechanisms in the black box

Journal of Molecular and Cellular Cardiology

Volumn 38, Issue 6, 2005, Pages 965-968

  Zhu, Zheng I ^a   Clancy, Colleen E ^a  

^a WEILL CORNELL MEDICAL COLLEGE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM; SODIUM CHANNEL; VOLTAGE GATED SODIUM CHANNEL;

ALPHA CHAIN; AUTOSOMAL RECESSIVE INHERITANCE; BRUGADA SYNDROME; CLINICAL FEATURE; ECG ABNORMALITY; EDITORIAL; HEART DEPOLARIZATION; HEART ELECTROPHYSIOLOGY; HEART MUSCLE CONDUCTION DISTURBANCE; HEART REPOLARIZATION; HUMAN; LONG QT SYNDROME; PHENOTYPIC VARIATION; PRIORITY JOURNAL; QRS COMPLEX; QT PROLONGATION; SICK SINUS SYNDROME; SODIUM CURRENT; ST SEGMENT ELEVATION; STEADY STATE; SYNCOPE; TORSADE DES POINTES;

ANIMALS; DNA; GENOME; HUMANS; IONS; LONG QT SYNDROME; MODELS, BIOLOGICAL; MUTATION; PHENOTYPE; PROTEIN STRUCTURE, TERTIARY; SODIUM; SODIUM CHANNELS; SYNDROME;

EID: 19444377690     PISSN: 00222828     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.yjmcc.2005.03.011     Document Type: Editorial

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