Clinical and molecular characterization of non-syndromic retinal dystrophy due to c.175G>A mutation in ceroid lipofuscinosis neuronal 3 (CLN3)

Overview of attention for article published in Documenta Ophthalmologica, November 2018

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Documenta #Ophthalmologica https://t.co/PhxHicTk3G A #CLN3 #mutation associated with #retinaldystrophy leading to #rod & delayed primary #cone #degeneration #ISCEV #ISCEVstandard #retina #lipofuscinosis #RetinitisPigmentosa #vision #electrophysiolog

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