Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2). [electronic resource]
Producer: 20010405Description: 189-94 p. digitalISSN:- 0964-6906
- 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
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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