Familial cerebral cavernous malformations associated with a splice-site CCM2 deletion

J Neurol. 2009 Jan;256(1):137-8. doi: 10.1007/s00415-009-0070-8. Epub 2009 Feb 9.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Aged
  • Brain / pathology*
  • Carrier Proteins / genetics*
  • Cavernous Sinus / pathology*
  • Family
  • Humans
  • Intracranial Arteriovenous Malformations / diagnosis
  • Intracranial Arteriovenous Malformations / genetics*
  • Intracranial Arteriovenous Malformations / pathology*
  • Magnetic Resonance Imaging
  • Male
  • Pedigree
  • Sequence Deletion*

Substances

  • CCM2 protein, human
  • Carrier Proteins