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Identification of a novel exon3 deletion of RYR2 in a family with catecholaminergic polymorphic ventricular tachycardia
BACKGROUND: RYR2, encoding cardiac ryanodine receptor, is the major responsible gene for catecholaminergic polymorphic ventricular tachycardia (CPVT). Meanwhile, KCNJ2, encoding inward‐rectifier potassium channel (I(K1)), can be the responsible gene for atypical CPVT. We recently encountered a famil...
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| Veröffentlicht in: | Ann Noninvasive Electrocardiol |
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| Hauptverfasser: | , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
John Wiley and Sons Inc.
2019
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6850420/ https://ncbi.nlm.nih.gov/pubmed/30615235 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/anec.12623 |
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