Cite
HARVARD Citation
Takayama, K. et al. (n.d.). 1218Double mutations in RYR2 cause severe phenotype of catecholaminergic polymorphic ventricular tachycardia. European heart journal. p. . [Online].
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Takayama, K. et al. (n.d.). 1218Double mutations in RYR2 cause severe phenotype of catecholaminergic polymorphic ventricular tachycardia. European heart journal. p. . [Online].