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Epilepsy, Myoclonic, Benign Adult Familial, Type 2 [Supplementary Concept]

Date introduced: November 5, 2012

MeSH Unique ID: C564313

Heading Mapped to:

Entry Terms:

  • BAFME2
  • Epilepsy, Familial Adult Myoclonic 2
  • FAME2
  • Benign Adult Familial Myoclonic Epilepsy 2
  • Cortical Myoclonus And Epilepsy, Autosomal Dominant

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