Autosomal dominant optic atrophy and cataract "plus" phenotype including axonal neuropathy (2019)

First Author: Horga A

Attributed to: MICA: MRC Centre for Neuromuscular Diseases funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/nxg.0000000000000322

PubMed Identifier: 31119193

Publication URI: http://europepmc.org/abstract/MED/31119193

Type: Journal Article/Review

Parent Publication: Neurology Genetics

Issue: 2

ISSN: 2376-7839