A rare mutation in EIF2B4 gene in an epileptic child with vanishing white matter disease: a case report. [electronic resource]

By: Contributor(s): Producer: 20150619Description: 41-6 p. digitalISSN:
  • 1015-8146
Subject(s): In: Genetic counseling (Geneva, Switzerland) vol. 26
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Publication Type: Case Reports; Journal Article

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