Clara Esteban-Jurado MSc, Maria Vila-Casadesús MSc, Pilar Garre MD, PhD, Juan José Lozano PhD, Anna Pristoupilova MSc, Sergi Beltran PhD, Jenifer Muñoz MSc, Teresa Ocaña MSc, Francesc Balaguer MD, PhD, Maria López-Cerón MD, PhD, Miriam Cuatrecasas MD, PhD, Sebastià Franch-Expósito MSc, Josep M. Piqué MD, PhD, Antoni Castells MD, PhD, Angel Carracedo MD, PhD, Clara Ruiz-Ponte PhD, Anna Abulí PhD, Xavier Bessa MD, PhD, Montserrat Andreu MD, PhD, Luis Bujanda MD, PhD, Trinidad Caldés PhD and Sergi Castellví-Bel PhD the EPICOLON Consortium
Genet Med 2014; advance online publication, July 24, 2014; doi:10.1038/gim.2014.89
In the originally published version of Figure 2, two plus signs were mistakenly omitted. The correct version appears on the following page. The publisher regrets the error.
Additional information
The online version of the original article can be found at 10.1038/gim.2014.89
Rights and permissions
About this article
Cite this article
Erratum: Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer. Genet Med 16, 988–989 (2014). https://doi.org/10.1038/gim.2014.126
Published:
Issue Date:
DOI: https://doi.org/10.1038/gim.2014.126
