Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology
- PMID: 32004434
- DOI: 10.1161/CIRCGEN.119.002824
Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology
Keywords: atrial fibrillation; cardiomyopathies; disease; genes; prognosis.
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