Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome

J Med Genet. 2004 May;41(5):323-6. doi: 10.1136/jmg.2004.018036.
No abstract available

Publication types

  • Review

MeSH terms

  • Gene Frequency
  • Germ-Line Mutation*
  • Hamartoma Syndrome, Multiple / diagnosis*
  • Hamartoma Syndrome, Multiple / genetics*
  • Humans
  • PTEN Phosphohydrolase
  • Phosphoric Monoester Hydrolases / genetics*
  • Tumor Suppressor Proteins / genetics*

Substances

  • Tumor Suppressor Proteins
  • Phosphoric Monoester Hydrolases
  • PTEN Phosphohydrolase
  • PTEN protein, human

Associated data

  • OMIM/158350