Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2).
Tiso, N
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2). [electronic resource] - Human molecular genetics Feb 2001 - 189-94 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0964-6906
10.1093/hmg/10.3.189 doi
Amino Acid Sequence
Arrhythmogenic Right Ventricular Dysplasia--genetics
Base Sequence
Chromosome Mapping
Chromosomes, Human, Pair 1--genetics
DNA--chemistry
DNA Mutational Analysis
Family Health
Female
Genetic Predisposition to Disease--genetics
Humans
Male
Molecular Sequence Data
Mutation
Mutation, Missense
Myocardium--metabolism
Pedigree
Polymorphism, Single-Stranded Conformational
Ryanodine Receptor Calcium Release Channel--genetics
Sequence Alignment
Sequence Homology, Amino Acid
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2). [electronic resource] - Human molecular genetics Feb 2001 - 189-94 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0964-6906
10.1093/hmg/10.3.189 doi
Amino Acid Sequence
Arrhythmogenic Right Ventricular Dysplasia--genetics
Base Sequence
Chromosome Mapping
Chromosomes, Human, Pair 1--genetics
DNA--chemistry
DNA Mutational Analysis
Family Health
Female
Genetic Predisposition to Disease--genetics
Humans
Male
Molecular Sequence Data
Mutation
Mutation, Missense
Myocardium--metabolism
Pedigree
Polymorphism, Single-Stranded Conformational
Ryanodine Receptor Calcium Release Channel--genetics
Sequence Alignment
Sequence Homology, Amino Acid