Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency: A Novel Mutation with Prominent Ataxia. [electronic resource]

By: Contributor(s): Publication details: Movement disorders clinical practice Description: 330-332 p. digitalISSN:
  • 2330-1619
Online resources: In: Movement disorders clinical practice vol. 5
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Publication Type: Case Reports; Journal Article

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