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Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models

Crossref DOI link: https://doi.org/10.1038/s41436-018-0018-4

Published Print: 2019-01

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Hart, Steven N.

Hoskin, Tanya

Shimelis, Hermela

Moore, Raymond M.

Feng, Bingjian

Thomas, Abigail

Lindor, Noralane M.

Polley, Eric C.

Goldgar, David E.

Iversen, Edwin

Monteiro, Alvaro N.A.

Suman, Vera J.

Couch, Fergus J.
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Text and Data Mining valid from 2019-01-01

Text and Data Mining valid from 2019-01-01

Version of Record valid from 2022-01-19
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This article is maintained by: Elsevier

Article Title: Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction models

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0018-4

Content Type: article

Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics