Population
Two families with autosomal-dominant non-compaction cardiomyopathy (NCCM)
Design
Case_series
Authors
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MYH7 mutations may underlie familial NCCM; extends sarcomeric cardiomyopathy spectrum but remains hypothesis-generating and should not yet change practice.
Mutations in the MYH7 gene are associated with non-compaction cardiomyopathy, linking its genetic etiology to hypertrophic, restrictive, and dilated cardiomyopathies.
Hoedemaekers et al. (2007) studied this question.
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