Cite
HARVARD Citation
Winnik, S. et al. (n.d.). P1799Identification of a novel gene mutation in TRPM4 in a family with premature SCD, cardiac conduction disease and cardiomyopathy. European heart journal. p. . [Online].
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Winnik, S. et al. (n.d.). P1799Identification of a novel gene mutation in TRPM4 in a family with premature SCD, cardiac conduction disease and cardiomyopathy. European heart journal. p. . [Online].