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Your search keyword '"Dooijes D"' showing total 6 results

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6 results on '"Dooijes D"'

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1. Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy*

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*

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