ArticleAnnals of pediatric cardiology
Biallelic truncating variants in the myosin-binding protein C3 result in a fatal form of cardiomyopathy in Indian infants.
Article in Annals of pediatric cardiology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
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.
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