Lack of S37A CTNNB1/β-catenin mutations in a Swedish cohort of 98 parathyroid adenomas

Clin Endocrinol (Oxf). 2010 Oct;73(4):552-3. doi: 10.1111/j.1365-2265.2010.03830.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adenoma / genetics*
  • Adult
  • Aged
  • Aged, 80 and over
  • Cohort Studies
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mutation*
  • Parathyroid Neoplasms / genetics*
  • Sweden
  • beta Catenin / genetics*

Substances

  • CTNNB1 protein, human
  • beta Catenin