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

doi:10.1097/WNO.0000000000002153

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 journal › Letter › peer-review

Original language	English (US)
Pages (from-to)	e105-e106
Journal	Journal of Neuro-Ophthalmology
Volume	45
Issue number	2
DOIs	https://doi.org/10.1097/WNO.0000000000002153
State	Published - Jun 2025
Externally published	Yes

ASJC Scopus subject areas

Ophthalmology
Clinical Neurology

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10.1097/WNO.0000000000002153

Cite this

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. / Mcannis, Kathryn E.; Ruiz-Montenegro, Alfredo; Davila, Pamela A. et al.
In: Journal of Neuro-Ophthalmology, Vol. 45, No. 2, 06.2025, p. e105-e106.

Research output: Contribution to journal › Letter › peer-review

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title = "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",

author = "Mcannis, \{Kathryn E.\} and Alfredo Ruiz-Montenegro and Davila, \{Pamela A.\} and Laylani, \{Noor A.\} and Lee, \{Andrew G.\}",

year = "2025",

month = jun,

doi = "10.1097/WNO.0000000000002153",

language = "English (US)",

volume = "45",

pages = "e105--e106",

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AU - Mcannis, Kathryn E.

AU - Ruiz-Montenegro, Alfredo

AU - Davila, Pamela A.

AU - Laylani, Noor A.

AU - Lee, Andrew G.

PY - 2025/6

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M3 - Letter

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AN - SCOPUS:105005454729

SN - 1070-8022

VL - 45

SP - e105-e106

JO - Journal of Neuro-Ophthalmology

JF - Journal of Neuro-Ophthalmology

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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

ASJC Scopus subject areas

Access to Document

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