Apparent homozygosity for p.E1841K mutation in a patient with MYH9-related disorder: a misdiagnosis for an autosomal dominant disorder?

Eur J Haematol. 2012 Apr;88(4):365-6. doi: 10.1111/j.1600-0609.2011.01746.x.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Humans
  • Male
  • Molecular Motor Proteins / genetics*
  • Myosin Heavy Chains / genetics*

Substances

  • Molecular Motor Proteins
  • Myosin Heavy Chains