📣 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.

The repeat variant in MSH3 is not a genetic modifier for spinocerebellar ataxia type 3 and Friedreich's ataxia. (2020)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awaa043

PubMed Identifier: 32154839

Publication URI: http://europepmc.org/abstract/MED/32154839

Type: Journal Article/Review

Volume: 143

Parent Publication: Brain : a journal of neurology

Issue: 4

ISSN: 0006-8950