Nuclear DNA Mutation Causing a Phenotypic Leber Hereditary Optic Neuropathy Plus.
Overview
publication date
- September 9, 2020
published in
- Ophthalmology Journal
Research
keywords
- DNA
- DNA, Mitochondrial
- Methyltransferases
- Mitochondrial Proteins
- Mutation
- Optic Atrophy, Hereditary, Leber
Identity
Scopus Document Identifier
- 85092651672
Digital Object Identifier (DOI)
- 10.1016/j.ophtha.2020.09.011
PubMed ID
- 32918965
Additional Document Info
has global citation frequency
volume
- 128
issue
- 4