Dominant ACO2 mutations are a frequent cause of isolated optic atrophy

Overview of attention for article published in Brain Communications, April 2021

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RT @braincomms: By screening European cohorts of individuals with genetically unsolved inherited optic neuropathies, Charif et al. report t…

By screening European cohorts of individuals with genetically unsolved inherited optic neuropathies, Charif et al. report the important contribution of ACO2 monoallelic pathogenic variants to dominant optic atrophy. @UnivAngers https://t.co/yCg6Psc4gM h…

Open Access UCL Research: Dominant ACO2 mutations are a frequent cause of isolated optic atrophy https://t.co/C2uzG8fHHC

Dominant ACO2 mutations are a frequent cause of isolated optic atrophy https://t.co/42Vbnfityx

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