Citations 2

Clinical Validity of Autosomal Dominant ALPK3 Loss-of-Function Variants as a Cause of Hypertrophic Cardiomyopathy

Circulation: Genomic and Precision Medicine | April 21, 2025 | Volume: 18 | Issue: 3 | Pages: No page available

10.1161/circgen.124.004976 | PMID 40255155

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

Europace | August 2, 2011 | Volume: 13 | Issue: 8 | Pages: 1077-1109

10.1093/europace/eur245 | PMID 21810866