P1580Catecholaminergic polymorphic ventricular tachycardia1 (CPVT1) with autosomal recessive inheritance, is caused by extremely rare RYR2 variant, presenting with cardiac arrest and VF

  • A. Shauer, Z. Perles, Y. Elitzur, A. Tashma, O. Elpeleg, D. Luria
  • EP Europace, June 2017, Oxford University Press (OUP)
  • DOI: 10.1093/ehjci/eux158.206

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http://dx.doi.org/10.1093/ehjci/eux158.206