Impairments in contractility and cytoskeletal organisation cause nuclear defects in nemaline myopathy. (2019)

First Author: Ross JA
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/10.1007/s00401-019-02034-8

PubMed Identifier: 31218456

Publication URI: http://europepmc.org/abstract/MED/31218456

Type: Journal Article/Review

Volume: 138

Parent Publication: Acta neuropathologica

Issue: 3

ISSN: 0001-6322