Correction: Møller, P.; et al. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11, 132

Pål Møller; Mev Dominguez-Valentin; Einar Andreas Rødland; Eivind Hovig

doi:10.3390/cancers12020410

Correction: Møller, P.; et al. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11, 132

Cancers (Basel). 2020 Feb 10;12(2):410. doi: 10.3390/cancers12020410.

Authors

Pål Møller^{1

2

3}, Mev Dominguez-Valentin¹, Einar Andreas Rødland¹, Eivind Hovig^{1

4}

Affiliations

¹ Department of Tumor Biology, Institute of Cancer Research, The Norwegian Radium Hospital, Part of Oslo University Hospital, 0424 Oslo, Norway.
² Center for Hereditary Tumors, HELIOS-Klinikum Wuppertal, University ofWitten-Herdecke, 42283 Wuppertal, Germany.
³ Department of Medical Genetics, The Norwegian Radium Hospital, Oslo University Hospital, 0424 Oslo, Norway.
⁴ Center for Bioinformatics, Department of Informatics, University of Oslo, PO box 1080, Blindern, 0316 Oslo, Norway.

Abstract

The authors wish to make the following corrections to this paper [1]: The authors would like to replace Table 3 in [1]. The corrections are correcting typographical errors when translating our database in BIC format to HGVS nomenclature, and removing four carriers which had zero follow-up time. [...].

Publication types

Published Erratum