Title
Correction: Causes for frequent pathogenic brca1 variants include low penetrance in fertile ages, recurrent de-novo mutations and genetic drift (Cancers, (2019), 11, 132, 10.3390/cancers11020132)
Date Issued
01 February 2020
Access level
open access
Resource Type
corrigendum
Author(s)
Møller P.
Rødland E.A.
Hovig E.
Part of Oslo University Hospital
Publisher(s)
MDPI AG
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. The original version of Table 3 is: (Table Presented) The authors would like to apologize for any inconvenience caused to the readers by these changes.
Volume
12
Issue
2
Language
English
OCDE Knowledge area
Bioquímica, Biología molecular Oncología
Scopus EID
2-s2.0-85079605659
Source
Cancers
ISSN of the container
20726694
Sources of information: Directorio de Producción Científica Scopus