Clinical case study meets population cohort: Identification of a BRCA1 pathogenic founder variant in Orcadians (2022)
Attributed to:
Determining the causal links and clinical significance of rare genetic variants
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1101/2022.07.18.22276644
Publication URI: http://dx.doi.org/10.1101/2022.07.18.22276644
Type: Preprint