A British family with familial cerebral cavernous malformation due to a rare mutation of the CCM2 gene. [electronic resource]

By: Contributor(s): Producer: 20210531Description: 1227-1229 p. digitalISSN:
  • 2240-2993
Subject(s): Online resources: In: Acta neurologica Belgica vol. 120
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Publication Type: Case Reports; Letter

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