A novel RYR2 missense mutation causing catecholaminergic polymorphic ventricular tachycardia and numerous sudden deaths. - Archive ouverte HAL Accéder directement au contenu
Communication Dans Un Congrès Année : 2017

A novel RYR2 missense mutation causing catecholaminergic polymorphic ventricular tachycardia and numerous sudden deaths.

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hal-04003560 , version 1 (24-02-2023)

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  • HAL Id : hal-04003560 , version 1

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M Blancard, L Yin, G Vaksmann, N Roux-Buisson, I Denjoy, et al.. A novel RYR2 missense mutation causing catecholaminergic polymorphic ventricular tachycardia and numerous sudden deaths.. Printemps de la Cardiologie, SFC, Apr 2017, Nantes (44000), France. ⟨hal-04003560⟩
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