Mutation of perinatal myosin heavy chain

N Engl J Med. 2004 Dec 9;351(24):2556-8; author reply 2556-8.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Arthrogryposis / genetics*
  • Fingers / abnormalities
  • Heart / embryology*
  • Humans
  • Mutation, Missense*
  • Myosin Heavy Chains / genetics*
  • Myxoma / genetics*
  • Pigmentation Disorders / genetics*
  • Syndrome
  • Trismus / genetics*

Substances

  • MYH8 protein, human
  • Myosin Heavy Chains