Uncommon MEN2A phenotype in a patient with a RET protooncogene exon 10, codon 611 mutation

Clin Endocrinol (Oxf). 2009 Aug;71(2):304-5. doi: 10.1111/j.1365-2265.2008.03475.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Codon*
  • Exons*
  • Female
  • Humans
  • Middle Aged
  • Multiple Endocrine Neoplasia Type 2a / diagnostic imaging
  • Multiple Endocrine Neoplasia Type 2a / genetics*
  • Mutation*
  • Phenotype
  • Proto-Oncogene Proteins c-ret / genetics*
  • Radionuclide Imaging

Substances

  • Codon
  • Proto-Oncogene Proteins c-ret