Whole exome sequencing in families with CLL detects a variant in Integrin β 2 associated with disease susceptibility

Blood. 2016 Nov 3;128(18):2261-2263. doi: 10.1182/blood-2016-02-697771. Epub 2016 Sep 14.
No abstract available

Publication types

  • Letter
  • Research Support, N.I.H., Extramural

MeSH terms

  • CD18 Antigens / genetics*
  • Case-Control Studies
  • Exome Sequencing
  • Family
  • Female
  • Genetic Predisposition to Disease*
  • Genetic Testing
  • Humans
  • Leukemia, Lymphocytic, Chronic, B-Cell / genetics*
  • Leukemia, Lymphocytic, Chronic, B-Cell / pathology
  • Male
  • Mutation, Missense*
  • Nuclear Proteins / genetics

Substances

  • CD18 Antigens
  • Nuclear Proteins
  • Swi5 protein, human