Hypertrophic cardiomyopathy family with double-heterozygous mutations; does disease severity suggest doubleheterozygosity?
I. A. W. van Rijsingen, J. F. Hermans-van Ast, Y. H. J. M. Arens, S. M. Schalla, C. E. M de Die-Smulders, A. van den Wijngaard, Y. M. PintoVolume:
17
Language:
english
Pages:
6
DOI:
10.1007/bf03086304
Date:
December, 2009
File:
PDF, 117 KB
english, 2009