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Germline Missense Variants in BRCA1: New Trends and Challenges for Clinical Annotation
Open AccessCorrection

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

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
*
Author to whom correspondence should be addressed.
Cancers 2020, 12(2), 410; https://doi.org/10.3390/cancers12020410
Received: 8 January 2020 / Revised: 6 February 2020 / Accepted: 6 February 2020 / Published: 10 February 2020
(This article belongs to the Special Issue BRCA Mutations and Cancer)
Note: In lieu of an abstract, this is an excerpt from the first page.

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. [...] View Full-Text
MDPI and ACS Style

Møller, P.; Dominguez-Valentin, M.; Rødland, E.A.; Hovig, E. 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 2020, 12, 410.

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