Nature Scientific reports, Vol. 10, Issue 1, Pages 20610, 2020

PMID: 33244021

The PRKAG2 syndrome is a rare autosomal dominant phenocopy of sarcomeric hypertrophic cardiomyopathy (HCM), characterized by ventricular pre- excitation, progressive conduction system disease and left ventricular hypertrophy. This study describes the phenotype, genotype and clinical outcomes of a South-Asian PRKAG2 cardiomyopathy cohort over a 7-year period.

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  https://www.ncbi.nlm.nih.gov/pubmed/33244021