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