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Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy
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Circulation: Genomic and Precision Medicine | April 21, 2025 | Volume: 18 | Issue: 3 | Pages: No page available
HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies
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Europace | August 2, 2011 | Volume: 13 | Issue: 8 | Pages: 1077-1109