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Updated: May 30, 2026

Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo
Published on: September 22, 2017
Absence of the OPTN mutation in a patient with ALS and familial primary open angle glaucoma
P Corcia1, J Praline, A M Guennoc
1Centre SLA, CHRU de Tours, Tours, France; UMR INSERM U930, Université François Rabelais de Tours, Tours, France. corcia@med.univ-tours.fr
Abstract:
The optineurin (OPTN) gene, known to be implicated in primary open-angle glaucoma (POAG), is the more recent genetic factor linked to ALS. We report the case of a 75year-old man who developed ALS and whose medical history was dominated by a familial POAG. The absence of OPTN gene mutation in a patient who suffered from two conditions linked to mutations of this gene does not support involvement of OPTN in ALS.
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