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Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia.
Nuchal Translucency Measurement
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Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia.
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation. 2001 Jan 30; 103(4):485-90.
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PubMed
subject areas
Base Sequence
Base Sequence
Chromosome Mapping
Chromosome Mapping
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 1
DNA
DNA
DNA Mutational Analysis
DNA Mutational Analysis
Family Health
Family Health
Female
Female
Finland
Finland
Haplotypes
Haplotypes
Humans
Humans
Male
Male
Microsatellite Repeats
Microsatellite Repeats
Mutation
Mutation
Mutation, Missense
Mutation, Missense
Myocardium
Myocardium
Pedigree
Pedigree
Polymorphism, Genetic
Polymorphism, Genetic
Ryanodine Receptor Calcium Release Channel
Ryanodine Receptor Calcium Release Channel
Tachycardia, Ventricular
Tachycardia, Ventricular
authors with profiles
Kevin Michael Brown