Albert Suurmeijer

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2014
Recurrent and founder mutations in the Netherlands: Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia
Van Der Zwaag, P. A., Cox, M. G. P. J., Van Der Werf, C., Wiesfeld, A. C. P., Jongbloed, J. D. H., Dooijes, D., Bikker, H., Jongbloed, R., Suurmeijer, A. J. H., Van Den Berg, M. P., Hofstra, R. M. W., Hauer, R. N. W., Wilde, A. A. M. & Van Tintelen, J. P., 1-Nov-2014, Founder Mutations in Inherited Cardiac Diseases in the Netherlands. Bohn Stafleu Van Loghum bv, p. 69-79 11 p.
Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review

Research output