Letters

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

  1. Dominique J. Verlaan BSc1,
  2. Sandra B. Laurent BTS1,
  3. Daniel L. Rochefort MSc1,
  4. Christina L. Liquori BS2,
  5. Douglas A. Marchuk PhD2,
  6. Adrian M. Siegel MD3,
  7. Guy A. Rouleau MD, PhD4

Article first published online: 26 APR 2004

DOI: 10.1002/ana.20112

Issue

Annals of Neurology

Annals of Neurology

Volume 55, Issue 5, pages 757–758, May 2004

Additional Information

How to Cite

Verlaan, D. J., Laurent, S. B., Rochefort, D. L., Liquori, C. L., Marchuk, D. A., Siegel, A. M. and Rouleau, G. A. (2004), CCM2 mutations account for 13% of cases in a large collection of kindreds with hereditary cavernous malformations. Ann Neurol., 55: 757–758. doi: 10.1002/ana.20112

Author Information

  1. 1

    Center for Research in Neurosciences and Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada

  2. 2

    Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC

  3. 3

    Epilepsy Program, Department of Neurology, University Hospital, Züurich, Switzerland

  4. 4

    Center for Research in Neurosciences, Montreal General Hospital and Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada

Publication History

  1. Issue published online: 26 APR 2004
  2. Article first published online: 26 APR 2004

Funded by

  • Quebec Health Research Fund Training and Support for Research (FRSQ-FCAR) scholarship
  • CIHR
  • Quebec Health Research Fund (FRSQ)

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