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Common variation in the NOS1AP gene is associated with drug-induced QT prolongation and ventricular arrhythmia
Long-QT syndrome and torsades de pointes in a patient with Takotsubo cardiomyopathy: an unusual case
Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.
Integration of genetic testing into diagnostic pathways for cardiomyopathies: a clinical consensus statement by the ESC Council on Cardiovascular Genomics
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndrome
