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

First Author: Horga A

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

Volume: 5

Parent Publication: Neurology. Genetics

Issue: 2

ISSN: 2376-7839