Why the study?
Is familial hypertrophic cardiomyopathy genetically heterogeneous?
Is familial hypertrophic cardiomyopathy genetically heterogeneous?
Familial hypertrophic cardiomyopathy is a genetically heterogeneous disorder caused by defects in at least two distinct loci.
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Requires consideration of multiple loci when evaluating FHC families; leaves open mapping of additional causative genes.
Solomon et al. (1990) studied this question.