Retinal dystrophy associated with a single-base deletion mutation in mitochondrial DNA 3271 in patient with MELAS syndrome

Overview of attention for article published in Documenta Ophthalmologica, January 2019

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RT @ClinMedJournals: Documenta #Ophthalmologica https://t.co/PR5sPwMwg8 #RetinalDystrophy due to a #mutation in #mtDNA in #MELAS syndrome…

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Documenta #Ophthalmologica https://t.co/PR5sPwMwg8 #RetinalDystrophy due to a #mutation in #mtDNA in #MELAS syndrome #Retina # #Retinopathy #electrophysiology #Vision #ERG #VEP #ISCEV https://t.co/eSz8CjQof1

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Retinal dystrophy associated with a single-base deletion mutation in mitochondrial DNA 3271 in patient with MELAS syndrome. https://t.co/yX0LnrS0F8

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Retinal dystrophy associated with a single-base deletion mutation in mitochondrial DNA 3271 in patient with MELAS syndrome. https://t.co/Zkr9Te5gjv https://t.co/xldKafbi97

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