Biallelic truncating variants in the Myosin-Binding Protein C3 gene resulted in a fatal form of cardiomyopathy in four Indian infants.
Biallelic truncating variants in the Myosin-Binding Protein C3 gene are associated with a fatal form of pediatric cardiomyopathy.
Absolute Event Rate: 0% vs 0%
As the genetic basis of pediatric cardiomyopathies is widely understood, it is hoped that the genotype would provide prognostic information about the course of the disease. We report four Indian infants with a fatal form of cardiomyopathy due to biallelic truncating variants in the Myosin-Binding Protein C3 gene.
Krishna et al. (Sat,) reported a other. Biallelic truncating variants in the Myosin-Binding Protein C3 gene resulted in a fatal form of cardiomyopathy in four Indian infants.