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. Issue 1 (14th March 2022) - Saffra, Norman A.; Emborgo, Trisha S.; Laureta, Emma C.; Kirsch, David S.; Guarini, Ludovico
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