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- W2585346723 abstract "Sudden infant death syndrome (SIDS) is the primary cause of postneonatal mortality in the United States and the third leading cause of infant death. Mutations in the RyR2-encoded cardiac ryanodine receptor/calcium release cause the highly lethal and unsuspecting catecholaminergic polymorphic ventricular tachycardia (CPVT1) in the young. We sought to determine the spectrum and prevalence of RyR2 mutations in a large cohort of SIDS by performing postmortem genetic testing." @default.
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- W2585346723 date "2006-05-01" @default.
- W2585346723 modified "2023-09-23" @default.
- W2585346723 title "AB32-4" @default.
- W2585346723 doi "https://doi.org/10.1016/j.hrthm.2006.02.211" @default.
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