📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

FILIP1-associated neuromuscular disorder and phenotypic blending due to paternal UPD6. (2024)

First Author: Watts LM

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/10.1093/braincomms/fcae330

PubMed Identifier: 39386087

Publication URI: http://europepmc.org/abstract/MED/39386087

Type: Journal Article/Review

Volume: 6

Parent Publication: Brain communications

Issue: 5

ISSN: 2632-1297