Cranial, axial and proximal myopathy and hypertrophic cardiomyopathy caused by a mutation in the globular head region of the MYH7 gene

Eur J Neurol. 2014 Jun;21(6):e51-2. doi: 10.1111/ene.12416.
No abstract available

Keywords: Laing disease; MYH7 gene; axial weakness; cardiomyopathy; muscle dystrophy.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Cardiac Myosins / genetics*
  • Cardiomyopathy, Hypertrophic / genetics*
  • Female
  • Humans
  • Middle Aged
  • Muscular Diseases / genetics*
  • Mutation
  • Myosin Heavy Chains / genetics*


  • MYH7 protein, human
  • Cardiac Myosins
  • Myosin Heavy Chains