Population
Patients with inherited cardiomyopathies including hypertrophic cardiomyopathy, arrythmogenic right/left…
Design
Review
Authors
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Non-coding variants merit research prioritization in cardiomyopathies; leaves open their diagnostic or therapeutic utility pending validation.
This review highlights the role of mutations in non-coding regions of the genome, including microRNAs and long non-coding RNAs, in the pathogenesis of inherited cardiomyopathies.
Salman et al. (2018) studied this question.
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