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Rare disease gene association discovery from burden analysis of the 100,000 Genomes Project data. (2023)

First Author: Cipriani V

Attributed to: Identifying New Disease Genes & Mechanisms for Musculoskeletal Disorders in 100K Genomes Project using Bioinformatics, Phenotyping & Machine Learning funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1101/2023.12.20.23300294

PubMed Identifier: 38196618

Publication URI: http://europepmc.org/abstract/MED/38196618

Type: Journal Article/Review

Parent Publication: medRxiv : the preprint server for health sciences