Improved Locus‐Specific Database for OPA1 Mutations Allows Inclusion of Advanced Clinical Data
M Ferré, A Caignard, D Milea, S Leruez… - Human …, 2015 - Wiley Online Library
Autosomal‐dominant optic atrophy (ADOA) is the most common inherited optic neuropathy,
due to mutations in the optic atrophy 1 gene (OPA 1) in about 60%–80% of cases. At …
due to mutations in the optic atrophy 1 gene (OPA 1) in about 60%–80% of cases. At …