📣 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.

Incomplete annotation has a disproportionate impact on our understanding of Mendelian and complex neurogenetic disorders (2020)

First Author: Zhang D

Attributed to: Understanding the genes for Parkinson's disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1126/sciadv.aay8299

PubMed Identifier: 32917675

Publication URI: http://europepmc.org/abstract/MED/32917675

Type: Journal Article/Review

Parent Publication: Science Advances

Issue: 24

ISSN: 2375-2548