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Volumn 1, Issue 2, 2008, Pages 83-92
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Molecular and clinical characterization of a novel SCN5A mutation associated with atrioventricular block and dilated cardiomyopathy.
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Author keywords
[No Author keywords available]
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Indexed keywords
ALANINE;
MUSCLE PROTEIN;
SCN5A PROTEIN, HUMAN;
SODIUM CHANNEL;
VALINE;
ADULT;
AMINO ACID SUBSTITUTION;
ARTICLE;
ASIAN;
ATRIOVENTRICULAR BLOCK;
CELL LINE;
COMPARATIVE STUDY;
CONGESTIVE CARDIOMYOPATHY;
DISEASE COURSE;
ELECTROCARDIOGRAPHY;
ELECTROPHYSIOLOGY;
ETHNOLOGY;
EXERCISE TEST;
FEMALE;
GENETICS;
HEMODYNAMICS;
HUMAN;
MALE;
MIDDLE AGED;
MOLECULAR GENETICS;
NUCLEOTIDE SEQUENCE;
PATHOPHYSIOLOGY;
PEDIGREE;
SINGLE NUCLEOTIDE POLYMORPHISM;
ADULT;
ALANINE;
AMINO ACID SUBSTITUTION;
ASIAN CONTINENTAL ANCESTRY GROUP;
ATRIOVENTRICULAR BLOCK;
BASE SEQUENCE;
CARDIOMYOPATHY, DILATED;
CELL LINE;
DISEASE PROGRESSION;
ELECTROCARDIOGRAPHY;
ELECTROPHYSIOLOGY;
EXERCISE TEST;
FEMALE;
HEMODYNAMICS;
HUMANS;
MALE;
MIDDLE AGED;
MOLECULAR SEQUENCE DATA;
MUSCLE PROTEINS;
PEDIGREE;
POLYMORPHISM, SINGLE NUCLEOTIDE;
SODIUM CHANNELS;
VALINE;
YOUNG ADULT;
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EID: 65649123138
PISSN: None
EISSN: 19413084
Source Type: Journal
DOI: 10.1161/CIRCEP.107.750752 Document Type: Article |
Times cited : (76)
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References (0)
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