Current and future therapeutic approaches to the congenital myopathies (2017)

First Author: Jungbluth H
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/10.1016/j.semcdb.2016.08.004

PubMed Identifier: 27515125

Publication URI: http://europepmc.org/abstract/MED/27515125

Type: Journal Article/Review

Parent Publication: Seminars in Cell & Developmental Biology

ISSN: 1084-9521