Absence of a Primary Role for SCN10A Mutations in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. [electronic resource]
Producer: 20161213Description: 87-9 p. digitalISSN:- 1937-5395
- Adult
- Arrhythmogenic Right Ventricular Dysplasia -- diagnosis
- Case-Control Studies
- DNA Mutational Analysis
- Female
- Gene Frequency
- Genetic Association Studies
- Genetic Markers
- Genetic Predisposition to Disease
- Humans
- Male
- Middle Aged
- Mutation
- NAV1.8 Voltage-Gated Sodium Channel -- genetics
- Phenotype
- Risk Factors
- Young Adult
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Publication Type: Letter; Research Support, Non-U.S. Gov't
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