STEMOD™ CPVT1 Disease Model (RYR2, P2328S)

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  • Published date: January 26, 2021
    • United States

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited life-threatening arrhythmia leading to syncope and sudden cardiac death at a young age. This disease cell model belongs to CPVT1, an autosomal dominant mutations (P2328S) occur in the RYR2 gene. Generating pluripotent stem cells from foreskin fibroblasts, then differentiate into cardiac myocytes. This disease cell model provides a platform to explore disease mechanisms in human genetic cardiac disorders.https://www.creative-biolabs.com/stem-cell-therapy/cpvt1-disease-model-ryr2-p2328s-42.htm

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Jerry Carter
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