PRKAG2 and Fabry disease: Wang et al. analyzed 105 HCM patients who underwent genetic testing for eight HCM-associated sarcomere genes (myosin-binding protein C (MYBPC3), β-myosin heavy chain (MYH7), essential and regulatory myosin light chains, cardiac troponin T, cardiac troponin I, α-tropomyosin, and cardiac actin) and three HCM phenocopy genes (LAMP2 for Danon disease, GLA for Fabry disease, and PRKAG2 for PRKAG2 cardiomyopathy) along with CMR.