MYH2 mutation in recessive myopathy with external ophthalmoplegia linked to chromosome 17p13.1-p12

Brain. 2013 Jul;136(Pt 7):e238. doi: 10.1093/brain/aws365. Epub 2013 Feb 6.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Adult
  • Chromosomes, Human, Pair 17 / genetics*
  • Family Health
  • Female
  • Humans
  • Male
  • Middle Aged
  • Muscular Diseases / complications
  • Muscular Diseases / genetics*
  • Mutation / genetics*
  • Myosin Heavy Chains / genetics*
  • Ophthalmoplegia / complications
  • Ophthalmoplegia / genetics*
  • Young Adult

Substances

  • Myosin Heavy Chains