Duchenne muscular dystrophy patients lacking the dystrophin isoforms Dp140 and Dp71 and mouse models lacking Dp140 have a more severe motor phenotype

Summary

This is a publication. If there is no link to the publication on this page, you can try the pre-formated search via the search engines listed on this page.

Authors: Francesco Muntoni and Mary Chessyre (UCL)

Journal title:  Journal of Cachexia, Sarcopenia and Muscle

Journal publisher: Wiley

Published year: 2022

DOI identifier: 10.1002/jcsm.12914

ISSN: 2190-6009