Nuclear DNA Mutation Causing a Phenotypic Leber Hereditary Optic Neuropathy Plus. uri icon

Overview

publication date

  • September 9, 2020

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

volume

  • 128

issue

  • 4