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

Publication URI: http://dx.doi.org/10.1136/bmjno-2022-000352

Type: Journal Article/Review

Parent Publication: BMJ Neurology Open

Issue: 2