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Cardiac Sodium Channel Mutations: Why so Many Phenotypes?
M. Liu
, K. C. Yang
,
S. C. Dudley
Research output
:
Chapter in Book/Report/Conference proceeding
›
Chapter
19
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Scopus citations
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Dive into the research topics of 'Cardiac Sodium Channel Mutations: Why so Many Phenotypes?'. Together they form a unique fingerprint.
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Keyphrases
Sodium Channel mutation
100%
Cardiac Sodium Channel
100%
Nav1.5
100%
Phenotypic Variability
42%
Circadian Rhythm
14%
Loss Function
14%
Genetic Variation
14%
Atrial Fibrillation
14%
Genetic Modification
14%
Sick Sinus Syndrome
14%
Gain-of-function mutation
14%
Dilated Cardiomyopathy
14%
Genotype-phenotype
14%
Post-translational Modification
14%
Body Temperature
14%
Conduction Velocity
14%
Action Potential
14%
Na +
14%
Gene Transcription
14%
Action Potential Duration
14%
Complex Assembly
14%
Tissue Changes
14%
Penetrance
14%
Brugada Syndrome
14%
Impulse Propagation
14%
Genotype-phenotype Correlation
14%
Channel Function
14%
Heart Tissue
14%
Inward Current
14%
New Therapeutic Approaches
14%
RNA Processing
14%
Plateau Phase
14%
Na+ Channel
14%
Na+ Current
14%
Peak Current
14%
Upstroke
14%
Velocity Propagation
14%
Long QT Syndrome Type 3
14%
Gain Loss
14%
Late Na+ Current
14%
Cardiac Conduction Abnormalities
14%
Biochemistry, Genetics and Molecular Biology
Nav1.5
100%
Sodium Channel
100%
Posttranslational Modification
14%
Life Cycle
14%
Genetic Variation
14%
Genetic Transcription
14%
Action Potential
14%
Body Temperature
14%
RNA Processing
14%
Action Potential Duration
14%
Heart Conduction
14%
Penetrance
14%
RNA Transcription
14%
Gain of Function Mutation
14%
Sick Sinus Syndrome
14%
Brugada Syndrome
14%
Atrial Fibrillation
14%
Circadian Rhythm
14%
Long QT Syndrome
14%