A new centronuclear myopathy phenotype due to a novel dynamin 2 mutation

Neurology. 2009 Jan 6;72(1):93-5. doi: 10.1212/01.wnl.0000338624.25852.12.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • DNA Mutational Analysis
  • Dynamin II / genetics*
  • Female
  • Humans
  • Muscle, Skeletal / pathology
  • Mutation / genetics*
  • Myopathies, Structural, Congenital / genetics*
  • Myopathies, Structural, Congenital / pathology
  • Phenotype

Substances

  • Dynamin II