📣 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.

Expanding the Spectrum of AP5Z1- Related Hereditary Spastic Paraplegia ( HSP-SPG48 ): A Multicenter Study on a Rare Disease (2021)

First Author: Breza M

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/mds.28487

PubMed Identifier: 33543803

Publication URI: http://europepmc.org/abstract/MED/33543803

Type: Journal Article/Review

Parent Publication: Movement Disorders

Issue: 4

ISSN: 0885-3185