Clinical case study meets population cohort: identification of a BRCA1 pathogenic founder variant in Orcadians. (2023)
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/10.1038/s41431-023-01297-w
PubMed Identifier: 36927983
Publication URI: http://europepmc.org/abstract/MED/36927983
Type: Journal Article/Review
Volume: 31
Parent Publication: European journal of human genetics : EJHG
Issue: 5
ISSN: 1018-4813