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