Quantification of Sequence Exchange Events between PMS2 and PMS2CL Provides a Basis for Improved Mutation Scanning of Lynch Syndrome Patients

Heleen M. van der Klift, Carli M. J. Tops, Elsa C. Bik, Merel W. Boogaard, Anne-Marijke Borgstein, Kerstin B. M. Hansson, Margreet G. E. M. Ausems, Encarna Gomez Garcia, Andrew Green, Frederik J. Hes, Louise Izatt, Liselotte P. van Hest, Angel M. Alonso, Annette H. J. T. Vriends, Anja Wagner, Wendy A. G. van Zelst-Stams, Hans F. A. Vasen, Hans Morreau, Peter Devilee, Juul T. Wijnen

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)578-587
JournalHuman Mutation
Volume31
Issue number5
DOIs
Publication statusPublished - May 2010

Keywords

  • PMS2
  • PMS2CL
  • pseudogene
  • Lynch syndrome
  • HNPCC

Cite this

van der Klift, H. M., Tops, C. M. J., Bik, E. C., Boogaard, M. W., Borgstein, A-M., Hansson, K. B. M., Ausems, M. G. E. M., Garcia, E. G., Green, A., Hes, F. J., Izatt, L., van Hest, L. P., Alonso, A. M., Vriends, A. H. J. T., Wagner, A., van Zelst-Stams, W. A. G., Vasen, H. F. A., Morreau, H., Devilee, P., & Wijnen, J. T. (2010). Quantification of Sequence Exchange Events between PMS2 and PMS2CL Provides a Basis for Improved Mutation Scanning of Lynch Syndrome Patients. Human Mutation, 31(5), 578-587. https://doi.org/10.1002/humu.21229