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  • A developmental and epileptic encephalopathy characterized by X-linked dominant inheritance of seizure onset in the first months of life, intellectual disability, and poor motor control that has_material_basis_in mutation in the CDKL5 gene on chromosome Xp22.
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  • url:https://www.ncbi.nlm.nih.gov/pubmed/15492925
  • url:https://www.ncbi.nlm.nih.gov/pubmed/22872100
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