📣 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.

Comprehensive genetic diagnosis of tandem repeat expansion disorders with programmable targeted nanopore sequencing. (2022)

First Author: Stevanovski I

Attributed to: The AAGGG repeat expansion in RFC1 associated with late-onset ataxia and sensory neuropathy: from genetic cause to defining the functional mechanism funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1126/sciadv.abm5386

PubMed Identifier: 35245110

Publication URI: http://europepmc.org/abstract/MED/35245110

Type: Journal Article/Review

Volume: 8

Parent Publication: Science advances

Issue: 9

ISSN: 2375-2548