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A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutatedβ-myosin heavy chain genes

✍ Scribed by Brigitte Jeschke; Kerstin Uhl; Bernd Weist; Dirk Schröder; Thomas Meitinger; Christoph Döhlemann; H.-P. Vosberg

No coin nor oath required. For personal study only.

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