Gene symbol: RYR2. Disease: Arrhythmogenic right ventricular cardiomyopathy type 2

Authors :: Natascia Tiso
Bauce, B.
Rampazzo, A.
Bagattin, A.
Nava, A.
Danieli, G. A.
Source :: Europe PubMed Central, Scopus-Elsevier

Subjects :: Arrhythmogenic Right Ventricular Dysplasia/genetics
Amino Acid Substitution
RYR2
Genetic mutations
cardiomyopathy
Humans
Point Mutation
Ryanodine Receptor Calcium Release Channel
Codon
Arrhythmogenic Right Ventricular Dysplasia

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