Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.

Behr ER, Savio-Galimberti E, Barc J, Holst AG, Petropoulou E, Prins BP, Jabbari J, Torchio M, Berthet M, Mizusawa Y, Yang T, Nannenberg EA, Dagradi F, Weeke P, Bastiaenan R, Ackerman MJ, Haunso S, Leenhardt A, Kääb S, Probst V, Redon R, Sharma S, Wilde A, Tfelt-Hansen J, Schwartz P, Roden DM, Bezzina CR, Olesen M, Darbar D, Guicheney P, Crotti L, UK10K Consortium, Jamshidi Y
Cardiovasc Res. 2015 106 (3): 520-9

PMID: 25691538 · PMCID: PMC4447806 · DOI:10.1093/cvr/cvv042

MeSH Terms (27)

Action Potentials Adult Aged Brugada Syndrome 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 Male Middle Aged NAV1.8 Voltage-Gated Sodium Channel Odds Ratio Pedigree Phenotype Polymorphism, Single Nucleotide Risk Factors Saudi Arabia Transfection United States

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