Abnormal myosin post-translational modifications and ATP turnover time associated with human congenital myopathy-related RYR1 mutations (2023)

First Author: Sonne A

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/apha.14035

Publication URI: http://dx.doi.org/10.1111/apha.14035

Type: Journal Article/Review

Parent Publication: Acta Physiologica

Issue: 2