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