6 results on '"Dooijes D"'
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2. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands*
3. Recurrent and founder mutations in the Netherlands: Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia*
4. Recurrent and founder mutations in the Netherlands: Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia*.
5. Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy*.
6. Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands*.
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