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).

McAnnis, Kathryn E; Ruiz-Montenegro, Alfredo; Davila, Pamela A; Laylani, Noor A; Lee, Andrew G

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

Afiliação

McAnnis KE; Western University of Health Sciences (KEM), Lebanon, Oregon; Tecnológico de Monterrey (AR-M), Escuela de Medicina y Ciencias de la Salud, Monterrey, México; Department of Ophthalmology (PAD, NAL, AGL), Blanton Eye Institute, Houston Methodist Hospital, Houston, Texas; Departments of Ophthalmology, Neurology, and Neurosurgery (AGL), Weill Cornell Medicine, New York, New York; Department of Ophthalmology (AGL), University of Texas Medical Branch, Galveston, Texas; University of Texas MD Anderson

J Neuroophthalmol ; 2024 Apr 08.

Article em En | MEDLINE | ID: mdl-38587899

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article