A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutatedβ-myosin heavy chain genes
Brigitte Jeschke, Kerstin Uhl, Bernd Weist, Dirk Schröder, Thomas Meitinger, Christoph Döhlemann, H.-P. VosbergVolume:
102
Language:
english
Pages:
6
DOI:
10.1007/s004390050695
Date:
March, 1998
File:
PDF, 141 KB
english, 1998