📣 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.

Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis. (2016)

First Author: Gang Q

Attributed to: MICA: A UK-wide networking partnership to facilitate collaborative research in the idiopathic inflammatory myopathies funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.neurobiolaging.2016.07.024

PubMed Identifier: 27594680

Publication URI: http://europepmc.org/abstract/MED/27594680

Type: Journal Article/Review

Volume: 47

Parent Publication: Neurobiology of aging

ISSN: 0197-4580