Double nucleotidic mutation of the MYH9 gene in a young patient with end-stage renal disease

Nephrol Dial Transplant. 2004 Jan;19(1):249-51. doi: 10.1093/ndt/gfg475.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Female
  • Humans
  • Kidney Failure, Chronic / complications
  • Kidney Failure, Chronic / genetics*
  • Molecular Motor Proteins / genetics*
  • Mutation
  • Myosin Heavy Chains / genetics*
  • Nephritis, Hereditary / complications
  • Nephritis, Hereditary / genetics*

Substances

  • MYH9 protein, human
  • Molecular Motor Proteins
  • Myosin Heavy Chains