Asymptomatic Retinal Vein Occlusion in a 13-Year-Old with Heterozygous Deletion of the PMP22 Gene and a Diagnosis of Hereditary Neuropathy with Liability to Pressure Palsies

Norman A. Saffra, Trisha S. Emborgo, Emma C. Laureta, David S. Kirsch, Ludovico Guarini

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)E367-E370
JournalJournal of Neuro-Ophthalmology
Issue number1
StatePublished - 1 Mar 2022
Externally publishedYes

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