📣 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.

Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb. (2020)

First Author: Laitila JM

Attributed to: Determining how mutations in actin lead to skeletal muscle weakness funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s40478-020-0893-1

PubMed Identifier: 32066503

Publication URI: http://europepmc.org/abstract/MED/32066503

Type: Journal Article/Review

Volume: 8

Parent Publication: Acta neuropathologica communications

Issue: 1

ISSN: 2051-5960