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Volumn 109, Issue 5, 1997, Pages 504-511
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Molecular basis of the long-QT syndrome associated with deafness
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Author keywords
Arrhythmia; Deafness; Jervell and Lange Nielsen syndrome; KVLQT1; Long QT syndrome
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Indexed keywords
ADOLESCENT;
ADULT;
AGED;
CHILD;
CLINICAL ARTICLE;
CONFERENCE PAPER;
DISEASE ASSOCIATION;
DNA SEQUENCE;
FEMALE;
GENE MUTATION;
GENETIC ANALYSIS;
GENETIC LINKAGE;
HEARING IMPAIRMENT;
HUMAN;
LONG QT SYNDROME;
MALE;
PHENOTYPE;
ARTICLE;
BIOLOGICAL MODEL;
CASE REPORT;
CHROMOSOME 11;
CONSANGUINITY;
DOMINANT GENE;
GENETICS;
HETEROZYGOTE;
HOMOZYGOTE;
INFANT;
MIDDLE AGED;
MOLECULAR GENETICS;
MUTATION;
PEDIGREE;
PRESCHOOL CHILD;
RECESSIVE GENE;
SINGLE STRAND CONFORMATION POLYMORPHISM;
KCNQ1 PROTEIN, HUMAN;
POTASSIUM CHANNEL;
POTASSIUM CHANNEL KCNQ;
POTASSIUM CHANNEL KCNQ1;
VOLTAGE GATED POTASSIUM CHANNEL;
ADOLESCENT;
ADULT;
AGED;
AGED, 80 AND OVER;
CHILD;
CHILD, PRESCHOOL;
CHROMOSOMES, HUMAN, PAIR 11;
CONSANGUINITY;
DEAFNESS;
GENES, DOMINANT;
GENES, RECESSIVE;
HETEROZYGOTE;
HOMOZYGOTE;
HUMANS;
INFANT;
KCNQ POTASSIUM CHANNELS;
KCNQ1 POTASSIUM CHANNEL;
LOD SCORE;
LONG QT SYNDROME;
MIDDLE AGED;
MODELS, GENETIC;
MOLECULAR SEQUENCE DATA;
MUTATION;
PEDIGREE;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
POTASSIUM CHANNELS;
POTASSIUM CHANNELS, VOLTAGE-GATED;
SEQUENCE ANALYSIS, DNA;
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EID: 0031230388
PISSN: 1081650X
EISSN: None
Source Type: Journal
DOI: None Document Type: Conference Paper |
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Times cited : (14)
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References (28)
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