No abstract available
MeSH terms
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Adolescent
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Death, Sudden, Cardiac / etiology
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Female
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Genes, Dominant
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Heterozygote
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Humans
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KCNQ1 Potassium Channel / genetics*
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Long QT Syndrome / complications
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Long QT Syndrome / genetics*
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Male
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Pedigree
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Ryanodine Receptor Calcium Release Channel / genetics*
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Tachycardia, Ventricular / complications
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Tachycardia, Ventricular / genetics*
Substances
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KCNQ1 Potassium Channel
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KCNQ1 protein, human
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Ryanodine Receptor Calcium Release Channel