PuSH - Publication Server of Helmholtz Zentrum München

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1.
Behr, E.R.* et al.: Role of common and rare variants in SCN10A: Results from the Brugada syndrome QRS locus gene discovery collaborative study. Cardiovasc. Res. 106, 520-529 (2015)
2.
Sinner, M.F.* et al.: Integrating genetic, transcriptional, and functional analyses to identify five novel genes for atrial fibrillation. Circulation 130, 1225-1235 (2014)