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 (MOGAD).

Authors :: McAnnis KE
Ruiz-Montenegro A
Davila PA
Laylani NA
Lee AG
Source :: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society [J Neuroophthalmol] 2024 Apr 08. Date of Electronic Publication: 2024 Apr 08.
Publication Year :: 2024
Publisher :: Ahead of Print
Abstract: Competing Interests: The authors report no conflicts of interest.

Language :: English
ISSN :: 1536-5166
Database :: MEDLINE
Journal :: Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society
Publication Type :: Academic Journal
Accession number :: 38587899
Full Text :: https://doi.org/10.1097/WNO.0000000000002153

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