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Phenotypic expression and clinical outcomes in a South Asian PRKAG2 cardiomyopathy cohort

Scientific Reports, volume 10, Article number: 20610 (2020)

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.

  https://www.nature.com/articles/s41598-020-77124-9

 

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