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Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.

Maren F HansenJostein JohansenAnna E SylvanderInga BjørnevollBente A Talseth-PalmerLiss A S LavikAlexandre XavierLars F EngebretsenRodney J ScottFinn DrabløsWenche Sjursen
Published in: Clinical genetics (2017)
In conclusion, we found a promising DNA variant in more than 25 % of the patients, which shows that gene panel testing is a more effective method to identify germline variants in CRC patients compared to a single gene approach.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • newly diagnosed
  • chronic kidney disease
  • genome wide
  • prognostic factors
  • gene expression
  • dna methylation
  • dna damage
  • oxidative stress
  • single molecule