Associated Papers
Autosomal dominant optic atrophy: A novel treatment for OPA1 splice defects using U1 snRNA adaption.
Jüschke C et al.
Molecular Therapy. Nucleic Acids, 2021
Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families.
Pretegiani E et al.
Journal of the Neurological Sciences, 2017
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