Leber Hereditary Optic Neuropathy Plus Phenotype With Double Point Mutations (m.11778 G>A and m.14484T>C) and Concurrent Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease

Kathryn E. Mcannis, Alfredo Ruiz-Montenegro, Pamela A. Davila, Noor A. Laylani, Andrew G. Lee

Research output: Contribution to journalLetterpeer-review

Original languageEnglish (US)
Pages (from-to)e105-e106
JournalJournal of Neuro-Ophthalmology
Volume45
Issue number2
DOIs
StatePublished - Jun 2025
Externally publishedYes

ASJC Scopus subject areas

  • Ophthalmology
  • Clinical Neurology

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