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P1799Identification of a novel gene mutation in TRPM4 in a family with premature SCD, cardiac conduction disease and cardiomyopathy. (28th August 2018)
Record Type:
Journal Article
Title:
P1799Identification of a novel gene mutation in TRPM4 in a family with premature SCD, cardiac conduction disease and cardiomyopathy. (28th August 2018)
Main Title:
P1799Identification of a novel gene mutation in TRPM4 in a family with premature SCD, cardiac conduction disease and cardiomyopathy