No abstract available
MeSH terms
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Amino Acid Substitution
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Base Sequence
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Codon / genetics
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Humans
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Point Mutation
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Polymorphism, Genetic
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Ryanodine Receptor Calcium Release Channel / genetics*
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Tachycardia, Ventricular / genetics*
Substances
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Codon
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Ryanodine Receptor Calcium Release Channel