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Volumn 41, Issue 10, 2003, Pages 724-727
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A novel KCNQ1 mutation in Chinese with congenital long QT syndrome
a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
DNA;
KCNQ1 PROTEIN, HUMAN;
POTASSIUM CHANNEL;
POTASSIUM CHANNEL KCNQ;
POTASSIUM CHANNEL KCNQ1;
VOLTAGE GATED POTASSIUM CHANNEL;
ADOLESCENT;
ADULT;
ARTICLE;
CHEMISTRY;
CHILD;
COMPARATIVE STUDY;
ELECTROCARDIOGRAPHY;
FEMALE;
GENETIC POLYMORPHISM;
GENETICS;
HUMAN;
LONG QT SYNDROME;
MALE;
MIDDLE AGED;
MOLECULAR GENETICS;
MUTATION;
NUCLEOTIDE SEQUENCE;
PEDIGREE;
POLYMERASE CHAIN REACTION;
SINGLE STRAND CONFORMATION POLYMORPHISM;
ADOLESCENT;
ADULT;
BASE SEQUENCE;
CHILD;
DNA;
DNA MUTATIONAL ANALYSIS;
ELECTROCARDIOGRAPHY;
FEMALE;
HUMANS;
KCNQ POTASSIUM CHANNELS;
KCNQ1 POTASSIUM CHANNEL;
LONG QT SYNDROME;
MALE;
MIDDLE AGED;
MOLECULAR SEQUENCE DATA;
MUTATION;
PEDIGREE;
POLYMERASE CHAIN REACTION;
POLYMORPHISM, GENETIC;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
POTASSIUM CHANNELS;
POTASSIUM CHANNELS, VOLTAGE-GATED;
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EID: 2442713112
PISSN: 05781310
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (6)
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References (0)
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