No abstract available
MeSH terms
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Amino Acid Substitution
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Case-Control Studies
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Child
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Female
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Humans
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KCNQ1 Potassium Channel / genetics
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Long QT Syndrome / genetics*
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Muscle Proteins / genetics*
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Mutation, Missense
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NAV1.5 Voltage-Gated Sodium Channel
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Sodium Channels / genetics*
Substances
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KCNQ1 Potassium Channel
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KCNQ1 protein, human
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Muscle Proteins
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NAV1.5 Voltage-Gated Sodium Channel
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SCN5A protein, human
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Sodium Channels