Statistics for De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy
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| De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy | 0 |
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| December 2023 | 0 |
| January 2024 | 0 |
| February 2024 | 0 |
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| 13041_2021_Article_838.pdf | 27 |