Absence of a Primary Role for SCN10A Mutations in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.

Te Riele, Anneline S J M

Absence of a Primary Role for SCN10A Mutations in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy. [electronic resource] - Journal of cardiovascular translational research Feb 2016 - 87-9 p. digital

Publication Type: Letter; Research Support, Non-U.S. Gov't

1937-5395

10.1007/s12265-015-9670-0 doi


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