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Category: cyclin-dependent kinase-like 5 deficiency disorder

Researchers identify new treatment target for genetic epilepsy

The rare neurodevelopmental condition CDKL5 is characterised by early-onset epilepsy

February 10, 2024 CDKL5, cyclin-dependent kinase-like 5 deficiency disorder, Francis Crick Institute, genetic epilepsy, Loulou Foundation, News
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