A rare S33C mutation of CTNNB1 encoding β-catenin in a parathyroid adenoma found in an Italian primary hyperparathyroid cohort

Endocrine. 2012 Feb;41(1):152-5. doi: 10.1007/s12020-011-9558-y. Epub 2011 Nov 18.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoma / epidemiology
  • Adenoma / ethnology
  • Adenoma / genetics*
  • Aged
  • Cohort Studies
  • Comorbidity
  • Exons / genetics
  • Female
  • Humans
  • Hyperparathyroidism / epidemiology
  • Hyperparathyroidism / ethnology
  • Hyperparathyroidism / genetics*
  • Italy
  • Middle Aged
  • Mutation / genetics*
  • Parathyroid Neoplasms / epidemiology
  • Parathyroid Neoplasms / ethnology
  • Parathyroid Neoplasms / genetics*
  • Retrospective Studies
  • beta Catenin / genetics*

Substances

  • CTNNB1 protein, human
  • beta Catenin