Research output per year
Research output per year
Search results
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2014
Founder mutations in the Netherlands: Familial idiopathic ventricular fibrillation and DPP6
Postema, P. G., Christiaans, I., Hofman, N., Alders, M., Koopmann, T. T., Bezzina, C. R., Loh, P., Zeppenfeld, K., Volders, P. G. A. & Wilde, A. A. M., 1 Nov 2014, Founder Mutations in Inherited Cardiac Diseases in the Netherlands. Bohn Stafleu Van Loghum, p. 29-35 (Founder Mutations in Inherited Cardiac Diseases in the Netherlands).Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review
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Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide
Postema, P. G., van den Berg, M. P., van Tintelen, J. P., van den Heuvel, F., Grundeken, M., Hofman, N., van der Roest, W. P., Nannenberg, E. A., Krapels, I. P. C., Bezzina, C. R. & Wilde, A. A. M., 1 Nov 2014, Founder Mutations in Inherited Cardiac Diseases in the Netherlands. Bohn Stafleu Van Loghum, p. 21-27 (Founder Mutations in Inherited Cardiac Diseases in the Netherlands).Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review
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Recurrent and Founder Mutations in the Netherlands: The Long-QT Syndrome
Hofman, N., Jongbloed, R., Postema, P. G., Nannenberg, E., Alders, M. & Wilde, A. A. M., 1 Nov 2014, Founder Mutations in Inherited Cardiac Diseases in the Netherlands. Bohn Stafleu Van Loghum, p. 13-19 (Founder Mutations in Inherited Cardiac Diseases in the Netherlands).Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review