A novel mutation in ryanodine receptor 2 (RYR2) genes at c.12670G>T associated with focal epilepsy in a 3-year-old child

Overview of attention for article published in Frontiers in Pediatrics, October 2022

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New Research: A novel mutation in ryanodine receptor 2 (RYR2) genes at c.12670G>T associated with focal epilepsy in a 3-year-old child: Background Ryanodine receptor 2 (RYR2) encodes a component of a calcium channel. RYR2 variants were… https://t.co/EJ

24 Nov 2022

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