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Severe presentation and complex brain malformations in an individual carrying a CCND2 variant.

Gerarda CappuccioLorenzo UggaElena ParriniAlessandra D'AmicoNicola Brunetti-Pierri
Published in: Molecular genetics & genomic medicine (2019)
This report expands the phenotypic spectrum of the disorder due to CCND2 variants.
Keyphrases
  • white matter
  • copy number
  • resting state
  • early onset
  • case report
  • cerebral ischemia
  • multiple sclerosis
  • drug induced
  • brain injury
  • genome wide