Role of common and rare variants in SCN10A : results from the Brugada syndrome QRS locus gene discovery collaborative study - Behr, Elijah R.; Savio-Galimberti, Eleonora; Barc, Julien; Holst, Anders G.; Petropoulou, Evmorfia; Prins, Bram P.; Jabbari, Javad; Torchio, Margherita; Berthet, Myriam; Mizusawa, Yuka; Yang, Tao; Nannenberg, Eline A.; et al. (Cardiovascular research, 2015)
Keywords: Action Potentials; Adult; Aged; Brugada Syndrome - diagnosis; Brugada Syndrome - genetics; Brugada Syndrome - physiopathology; Case-Control Studies; Cell Line; Computational Biology; Databases, Genetic; DNA Mutational Analysis; Europe; Female; Gene Frequency; Genetic Association Studies; Genetic Predisposition to Disease; Heredity; Humans; Life Sciences; Male; Middle Aged; NAV1.8 Voltage-Gated Sodium Channel - genetics; NAV1.8 Voltage-Gated Sodium Channel - metabolism; Odds Ratio; Original; Pedigree; Phenotype; Polymorphism, Single Nucleotide; Risk Factors; Saudi Arabia; Transfection; United States; Saudi Arabia; United States; Europe; Genetics; SCN10A; QRS duration; Brugada syndrome; Rare variants; United States; Middle Aged; Genetic; Male; Case-Control Studies; Single Nucleotide; Saudi Arabia; Action Potentials; Databases; genetics; Transfection; DNA Mutational Analysis; Female; Odds Ratio; Cell Line; Genetic Predisposition to Disease; Genetic Association Studies; Gene Frequency; Risk Factors; Europe; Computational Biology; Heredity; Phenotype; NAV1.8 Voltage-Gated Sodium Channel; Pedigree; Aged; adult; humans; Polymorphism