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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

PubMed Identifier: 37602753

Publication URI: http://europepmc.org/abstract/MED/37602753

Type: Journal Article/Review

Volume: 239

Parent Publication: Acta physiologica (Oxford, England)

Issue: 2

ISSN: 1748-1708