CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations

Ann Neurol. 2004 May;55(5):757-8. doi: 10.1002/ana.20112.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cavernous Sinus / abnormalities*
  • Humans
  • Mutation*
  • Nervous System Malformations / epidemiology
  • Nervous System Malformations / genetics*