MSH2 Genomic Deletions Are a Frequent Cause of HNPCC

Nat Genet. 1998 Dec;20(4):326-8. doi: 10.1038/3795.

Publication types

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

MeSH terms

  • Base Pair Mismatch
  • Base Sequence
  • Colorectal Neoplasms, Hereditary Nonpolyposis / genetics*
  • DNA-Binding Proteins / genetics*
  • Exons
  • Gene Deletion*
  • Genetic Predisposition to Disease
  • Humans
  • MutS Homolog 2 Protein
  • Proto-Oncogene Proteins / genetics*

Substances

  • DNA-Binding Proteins
  • Proto-Oncogene Proteins
  • MSH2 protein, human
  • MutS Homolog 2 Protein