Changing faces of mitochondrial disease: autosomal recessive POLG disease mimicking myasthenia gravis and progressive supranuclear palsy. (2022)

First Author: Elwan M
Attributed to:  Pleiotropic disorders of mitochondrial translation funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/bmjno-2022-000352

PubMed Identifier: 36518302

Publication URI: http://europepmc.org/abstract/MED/36518302

Type: Journal Article/Review

Volume: 4

Parent Publication: BMJ neurology open

Issue: 2

ISSN: 2632-6140